Bill Text: MS HB1007 | 2022 | Regular Session | Introduced


Bill Title: Mississippi Medical Cannabis Compassion Act; create.

Spectrum: Partisan Bill (Republican 2-0)

Status: (Failed) 2022-02-01 - Died In Committee [HB1007 Detail]

Download: Mississippi-2022-HB1007-Introduced.html

MISSISSIPPI LEGISLATURE

2022 Regular Session

To: Drug Policy

By: Representatives Ford (73rd), McLean

House Bill 1007

AN ACT TO ENACT THE MISSISSIPPI MEDICAL CANNABIS COMPASSION ACT; TO AUTHORIZE MEDICAL CANNABIS USE BY CERTAIN PATIENTS WHO HAVE DEBILITATING MEDICAL CONDITIONS; TO PROVIDE FOR THE LEGISLATIVE INTENT; TO PROVIDE CERTAIN PROTECTIONS FOR QUALIFIED PATIENTS, DESIGNATED CAREGIVERS AND HEALTH CARE PRACTITIONERS; TO REQUIRE THE MISSISSIPPI DEPARTMENT OF HEALTH TO LICENSE AND REGULATE MEDICAL CANNABIS MANUFACTURERS; TO PROVIDE FOR THE LICENSING PROCESS FOR MEDICAL CANNABIS MANUFACTURERS AND SPECIALTY PHARMACIES; TO REQUIRE THE STATE BOARD OF PHARMACY TO LICENSE SPECIALTY PHARMACIES; TO REQUIRE MEDICAL CANNABIS SPECIALTY PHARMACIES AND QUALIFIED HEALTH CARE PRACTITIONERS TO COMPLY WITH THE PRESCRIPTION MONITORING PROGRAM; TO PROVIDE FOR A SEED-TO-SALE PROGRAM; TO REQUIRE THE DEPARTMENT OF HEALTH TO ESTABLISH AND ADMINISTER THE MISSISSIPPI MEDICAL CANNABIS PATIENT REGISTRY SYSTEM; TO ALLOW THE DEPARTMENT OF HEALTH TO SET THE MAXIMUM DAILY DOSAGE OF MEDICAL CANNABIS; TO SET CERTAIN REQUIREMENTS FOR THE SECURITY AND OPERATION OF MEDICAL CANNABIS MANUFACTURERS AND SPECIALTY PHARMACIES; TO ALLOW STATE-FUNDED PUBLIC UNIVERSITIES THE FIRST RIGHT OF REFUSAL TO BE LICENSED AS A MEDICAL CANNABIS MANUFACTURER; TO PROHIBIT ANY COMPANY FROM BEING LICENSED AS A MANUFACTURER OR SPECIALTY PHARMACY IF IT IS OWNED WHOLLY OR IN PART BY ANY STATE EMPLOYEE OR A MEMBER OF A STATE EMPLOYEE'S IMMEDIATE FAMILY; TO REQUIRE ALL EMPLOYEES OF MANUFACTURERS AND SPECIALTY PHARMACIES TO PASS A BACKGROUND CHECK; TO PROVIDE FOR VIOLATIONS OF THE ACT; TO SET LICENSING FEES OF MANUFACTURERS AND SPECIALTY PHARMACIES; TO PROVIDE FOR CERTAIN LIMITATIONS OF THE USE OF MEDICAL CANNABIS; TO REQUIRE THE BOARD OF PHARMACY AND THE DEPARTMENT OF HEALTH TO ADOPT RULES AND REGULATIONS RELATING TO MEDICAL CANNABIS; TO REQUIRE THAT THE DEPARTMENT OF HEALTH PROVIDE CERTAIN REPORTS TO THE LEGISLATURE REGARDING THE MEDICAL CANNABIS PROGRAM; TO ALLOW THE DEPARTMENT OF HEALTH AND BOARD OF PHARMACY TO EXAMINE THE BUSINESS AFFAIRS AND CONDITIONS OF MEDICAL CANNABIS MANUFACTURERS OR SPECIALTY PHARMACIES; TO PROHIBIT THE DEPARTMENT OF HEALTH AND BOARD OF PHARMACY FROM LICENSING SPECIALTY PHARMACIES AND MEDICAL CANNABIS MANUFACTURERS IN A COUNTY OR MUNICIPALITY UNLESS THE COUNTY OR MUNICIPALITY HAS AUTHORIZED THE OPERATION WITHIN ITS BOUNDARIES; TO PROVIDE THAT SPECIALTY PHARMACIES AND MEDICAL CANNABIS MANUFACTURERS SHALL COLLECT AND REMIT THE SALES TAX LEVIED IN SECTION 27-65-17(1)(a) FROM THE GROSS PROCEEDS DERIVED FROM EACH SALE OF MEDICAL CANNABIS; TO ESTABLISH THE MEDICAL CANNABIS RESEARCH AND OPPORTUNITY FUND IN THE STATE TREASURY; TO AMEND SECTIONS 25-53-5, 27-104-203, 27-65-111, 33-13-520, 41-29-125, 41-29-127, 41-29-136, 41-29-137, 41-29-139, 41-29-141, 41-29-143, 59-23-7, 63-11-30, 71-3-7, 71-3-121, 73-21-73, 73-21-127, 73-25-29 AND 83-9-22, MISSISSIPPI CODE OF 1972, TO CONFORM TO THE PROVISIONS OF THIS ACT; AND FOR RELATED PURPOSES.

     BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MISSISSIPPI:

     SECTION 1.  Title.  This chapter shall be known and may be cited as the "Mississippi Medical Cannabis Compassion Act."

     SECTION 2.  Legislative intent.  The Legislature finds and declares the following:

          (a)  It is not the intent of this chapter to provide for or enable recreational use of cannabis in the State of Mississippi.

          (b)  Establishing a program providing for the administration of cannabis derivatives for medical use in this state will not only benefit patients by providing relief to pain and other debilitating symptoms, but also provide opportunities for patients with these debilitating conditions to function and have a better quality of life.

          (c)  Allowing the cultivation, processing, dispensing and use of cannabis for medical use without appropriate safeguards to prevent unlawful diversion for recreational use would pose a risk to public health and safety.

          (d)  It is the intent of the Legislature to create within Mississippi a wholly intrastate system for the cultivation, processing and distribution of medical cannabis in the interest of protecting its own residents from the danger that recreational cannabis poses.

          (e)  The State of Mississippi, therefore, wishes to create a health care market for medical cannabis.

     SECTION 3.  Definitions.  For purposes of this chapter, unless the context requires otherwise, the following terms shall be defined as provided in this section:

          (a)  "Health care practitioner" means a Mississippi licensed doctor of medicine acting within the scope of authorized practice who has the primary responsibility for the care and treatment of a person diagnosed with a qualifying medical condition.

          (b)  "Intractable pain" means a pain state in which the cause of the pain cannot be removed or otherwise treated with the consent of the patient and which, in the generally accepted course of medical practice, no relief or cure of the cause of the pain is possible, or none has been found after reasonable efforts.  It is pain so chronic and severe as to otherwise warrant an opiate prescription.

          (c)  "MDOH" means the Mississippi Department of Health.          (d)  "Medical cannabis" means a medical grade product of any of the following, as determined by MDOH, that contains a derivate of cannabis for medical use by a registered qualifying patient pursuant to this chapter:

               (i)  Oral tablet, pill, capsule or tincture;

               (ii)  Gel, oil, cream or other topical preparation;

               (iii)  Suppository;

               (iv)  Transdermal patch; or

               (v)  Nebulizer or metered-dose inhaler.

     The term "medical cannabis" does not include any of the following:

               (i)  Raw plant material;

               (ii)  Any product administered by smoking, combustion or vaping;

               (iii)  A food product that has medical cannabis baked, mixed or otherwise infused into the product, such as cookies or candies.

          (e)  "Medical cannabis manufacturer" or "manufacturer" means an entity registered by the MDOH to cultivate, acquire, manufacture, possess, prepare, transfer, transport or supply  medical cannabis, delivery  devices, or related supplies and educational materials.

          (f)  "Medical cannabis product" means any delivery device or related supplies and educational materials used in the administration of medical cannabis for a patient with a qualifying medical condition enrolled in the program.

          (g)  "Patient registry" means an electronic integrated system that tracks practitioner certifications and recommendations, patient registrations, medical cannabis cards, the daily dosage and type of medical cannabis recommended to qualified patients by registered certifying practitioners, and the dates of sale, amounts and types of medical cannabis that were purchased by registered qualified patients at licensed specialty pharmacies.

          (h)  "Patient registry number" means a unique identification number assigned by the MDOH to a patient enrolled in the registry program.

          (i)  "Qualifying medical condition" means a diagnosis of any of the following conditions:

               (i)  Cancer, if the underlying condition or treatment produces one or more of the following:

                    1.  Severe or chronic pain;

                    2.  Nausea or severe vomiting, except for nausea related to cannabinoid hyperemesis syndrome; or

                    3.  Cachexia or severe wasting;

               (ii)  Glaucoma;

               (iii)  Human immunodeficiency virus or acquired immune deficiency syndrome;

               (iv)  Tourette's syndrome;

               (v)  Seizures, including those characteristics of epilepsy;

               (vi)  Severe and persistent muscle spasms, including those characteristic of multiple sclerosis;

               (vii)  Chron's disease;

               (viii)  Terminal illness, with a probable life expectancy of under one (1) year, if the illness or its treatment produces one or more of the following:

                    1.  Severe or chronic pain;

                    2.  Nausea or severe vomiting; or

                    3.  Cachexia or severe wasting;

               (ix)  Any of the following neurodegenerative diseases and conditions:

                    1.  Alzheimer's disease;

                    2.  Amyotrophic lateral sclerosis;

                    3.  Huntington's disease;

                    4.  Lewy body dementia;

                    5.  Motor neuron disease;

                    6.  Parkinson's disease;

                    7.  Spinal muscular atrophy;

               (x)  Spasticity;

               (xi)  Severe muscle spasms;

               (xii)  Intractable pain;

               (xiii)  Post traumatic stress disorder;

               (xiv)  Any of the following conditions associated with autism spectrum disorder, provided that the medical practitioner consults with a pediatric subspecialist if recommending medical cannabis to a patient under the age of eighteen (18):

                    1.  Repetitive or self-stimulatory behavior of such severity that the physical health of the person with autism is jeopardized; or

                    2.  Self-injuring behavior;

               (xv)  Traumatic brain injury;

               (xvi)  Chronic pain associated with fibromyalgia;

               (xvii)  Chronic pain associated with sickle cell disease;

               (xviii)  Any condition for which a patient is receiving hospice care or palliative care;

               (xix)  Ulcerative colitis;

               (xx)  Pain refractory to appropriate opioid management;

               (xxi)  Spinal cord disease or severe injury; and

               (xxii)  Any condition not otherwise specified in this chapter that a physician, in his or her medical opinion, considers debilitating to an individual patient and is qualified through his or her medical education and training to treat.

          (j)  "Qualified patient" means a Mississippi resident who has been diagnosed with a qualifying medical condition by a health care practitioner and has otherwise met any other requirements for patients under regulations set by the MDOH to participate in the program.

          (k)  "Recommendation" or "recommend" means an opinion of a health care practitioner licensed by and in good standing with the Mississippi State Board of Medical Examiners, provided within a bona fide doctor-patient relationship, that, in the sincere judgment of the practitioner, therapeutic cannabis may be helpful to the patient's condition or symptoms and is communicated by any means allowed by the MDOH.

          (l)  "Registered designated caregiver" means a person who:

               (i)  Is at least twenty-one (21) years old;

               (ii)  Does not have a conviction for a disqualifying felony offense;

               (iii)  Has been approved by the MDOH to assist a patient who has been identified by a health care practitioner as developmentally or physically disabled and therefore unable to self-administer or acquire medical cannabis from a distribution facility due to the disability; and

               (iv)  Is authorized by the MDOH to assist the patient with the use of medical cannabis.

          (m)  "Registry verification" means the verification provided by the MDOH that a patient is enrolled in the patient registry program and that includes the patient's name, patient registry number, recent photograph of the patient, the qualifying medical condition of the patient, and, if applicable, the name and photograph of the patient's registered designated caregiver, parent or legal guardian.

          (n)  "THC" or "Tetrahydrocannabinol" means any and all forms of tetrahydrocannabinol that are contained naturally in the cannabis plant, as well as synthesized forms of THC and derived variations, derivatives, isomers and allotropes that have similar molecular and physiological characteristics of tetrahydrocannabinol, including, but not limited to, THCA, THC Delta 9, THC Delta 8, THC Delta 10 and THC Delta 6.

     SECTION 4.  Authorization to use medical cannabis; requirements.  (1)  A resident of this state who is nineteen (19) years of age or older may be registered as a qualified patient if he or she meets all of the following conditions:

          (a)  Has been certified by a registered certifying health care practitioner as having a qualifying medical condition;

          (b)  Is registered with the MDOH; and

          (c)  Has been issued a valid medical cannabis card by the MDOH.

     (2)  A registered qualified patient may purchase, possess or use medical cannabis, subject to the other provisions of this chapter.  As a condition of continued enrollment as a registered qualified patient, the patient shall continue to receive regularly scheduled treatment for the patient's qualifying medical condition from his or her health care practitioner and shall report changes in the patient's qualifying medical condition to his or her health care practitioner.

     (3)  (a)  A resident of this state who is under the age of nineteen (19) years of age may be registered as a qualified patient if he or she meets all of the following conditions:

               (i)  Has been certified by a registered certifying physician as having a qualifying medical condition;

               (ii)  Is registered with the MDOH;

               (iii)  Has a qualified designated caregiver who is the patient's parent or legal guardian.

          (b)  A registered qualifying patient described in paragraph (a) of this subsection may use medical cannabis but shall not purchase medical cannabis.

     (4)  A resident of this state may be registered as a qualified caregiver if he or she meets all of the following conditions:

          (a)  Has registered with the MDOH;

          (b)  Has been issued a valid medical cannabis card by MDOH;

          (c)  Is at least twenty-one (21) years of age, unless he or she is the parent or legal guardian of, and caregiver for, a registered qualifying patient; and

          (d)  When applicable, is the parent, legal guardian, grandparent, spouse or an individual with power of attorney for health care of a registered qualified patient.

     (5)  A registered caregiver may purchase and possess medical cannabis but shall not use medical cannabis, unless he or she is also a registered qualified patient.

     (6)  In order for a health care practitioner to qualify as a registered certifying health care practitioner, he or she must meet the following requirements:

          (a)  Hold an active license to practice medicine in the state and be in good standing with the Mississippi State Board of Medical Licensure;

          (b)  Complete a four-hour course related to medical cannabis as offered by MDOH;

          (c)  Pay an initial registration fee established by MDOH, not to exceed Five Hundred Dollars ($500.00); and

          (d)  Meet any additional qualifications established by the MDOH.

     (7)  Upon meeting the requirements of subsection (6) of this section, MDOH shall issue a registration certificate and registration number to each registered certifying health care practitioner.  The MDOH shall maintain on its website an updated list of registered qualifying health care practitioners.

     (8)  The MDOH, by rule, may establish requirements for registered certifying health care practitioners to remain qualified, grounds for revoking registration and a process for renewing registration, including payment of an annual registration fee, not to exceed Five Hundred Dollars ($500.00).

     (9)  A registered certifying health care practitioner shall not do any of the following:

          (a)  Accept, solicit or offer any form of remuneration from or to a specialty pharmacy for the purpose of referring a patient to a specific specialty pharmacy;

          (b)  Offer a discount of any other item of value to a qualified patient who uses or agrees to designate a specific caregiver or use a specific specialty pharmacy to obtain medical cannabis;

          (c)  Hold a direct or indirect economic interest in a medical cannabis manufacturer or specialty pharmacy;

          (d)  Serve on the board of directors or as an employee of a medical cannabis manufacturer or specialty pharmacy;

          (e)  Refer qualified patients to a specific caregiver or a specific specialty pharmacy;

          (f)  Advertise in a specialty pharmacy;

          (g)  Advertise on the practitioner's website, brochures, billboards or any other media that generally describes the practice of the practitioner, any statement that refers to the practitioner as a "medical cannabis" or "medical marijuana" physician, practitioner or doctor, or otherwise advertises his or her status as a registered certifying practitioner, other than the following:

     "Dr. __________ is qualified and registered by the State of Mississippi to certify patients for medical cannabis under the Mississippi Medical Cannabis Compassion Act."

     (10)  A registered certifying health care practitioner may recommend medical cannabis to any patient suffering from a qualifying medical condition with whom he or she shares a bona fide doctor-patient relationship.  Before a patient's enrollment in the patient registry program, a health care practitioner shall:

          (a)  Determine, in the health care practitioner's medical judgment, whether a patient suffers from a qualifying medical condition, and, if so determined, provide the patient with a certification of that diagnosis;

          (b)  Determine whether a patient is developmentally or physically disabled and, as a result of that disability, the patient is unable to self-administer medication or acquire medical cannabis from a distribution facility, and, if so determined, include that determination on the patient's certification of diagnosis;

          (c)  Advise patients, registered designated caregivers, and parents or legal guardians who are acting as caregivers of the existence of any nonprofit patient support groups or organizations;

          (d)  Provide explanatory information from the MDOH to patients with qualifying medical conditions, including disclosure to all patients about the experimental nature of therapeutic use of medical cannabis; the possible risks, benefits, and side effects of the proposed treatment; the application and other materials from the MDOH; and

          (e)  Agree to continue treatment of the patient's qualifying medical condition and report medical findings to the MDOH.

     (11)  The health care practitioner shall analyze the patient's data in the Prescription Monitoring Program before recommending medical cannabis to the patient.  The health care practitioner may only recommend medical cannabis to a patient through an in-person medical appointment.  At the time of the health care practitioner's recommendation, a registered certifying health care practitioner shall enter electronically in the patient registry, in a manner determined by rule by the MDOH, relevant information necessary to appropriately identify the patient; the respective qualifying medical condition or conditions of the patient; the daily dosage and type of medical cannabis recommended for medical use; and any other information the MDOH, by rule, deems relevant.

     (12)  A registered certifying health care practitioner recommendation and certification of medical cannabis to a patient does not constitute a prescription for medical cannabis.

     (13)  A registered certifying health care practitioner recommendation and certification of medical cannabis shall be valid for a period of time as determined by the MDOH, but in no event may a practitioner's recommendation or certification exceed twelve (12) months in duration.

     (14)  The maximum daily dosage of medical cannabis shall be set by rule by the MDOH in consultation with qualified health care practitioners who wish to participate in the program.

     (15)  The maximum daily dosage may be increased under the following circumstance:  A registered certifying health care practitioner may increase a patient's daily dosage if the patient has been diagnosed with a terminal illness, provided that if the recommended daily dosage meets or exceeds seventy-five (75) milligrams of delta-9-tetrahydrocannabinol, the practitioner shall notify the patient that the patient's driver's license will be suspended.

     (16)  A registered certifying health care practitioner shall not lawfully recommend the use of medical cannabis with a potency greater than three percent (3%) tetrahydrocannabinol to any minor for any qualifying medical condition.  A minor shall not legally use medical cannabis with a potency greater than three percent (3%) tetrahydrocannabinol, whether or not the minor has a valid medical cannabis card.  A parent or legal guardian of a minor who holds a medical cannabis card shall not legally possess medical cannabis with potency greater than three percent (3%) tetrahydrocannabinol, unless the parent or guardian holds a valid medical cannabis card for his or her own qualifying medical condition.

     (17)  A registered certifying health care practitioner shall report adverse events and health outcomes associated with a patient's use of medical cannabis to the patient registry system.

     (18)  There is a presumption that a registered qualifying patient is engaged in the medical use of medical cannabis under this chapter if the person is in possession of a valid medical cannabis card and an amount of medical cannabis that does not exceed the maximum daily dosage of medical cannabis.  

     (19)  All employees, board of directors, shareholders and owners of medical cannabis manufacturers and specialty pharmacies, potential qualified patients and designated caregivers shall be citizens of the United States and shall provide their social security numbers to the MDOH and  State Board of Pharmacy, as applicable, upon their application and registration.

     (20)  After one hundred twenty (120) days from the effective date of this act, the MDOH and the State Board of Pharmacy shall issue licenses according to their respective duties as provided for in this chapter.

     SECTION 5.  Medical cannabis manufacturers.  (1)  The MDOH shall develop an annual, nontransferable specialty license for medical cannabis manufacturers for the production and manufacturing of cannabis for medical use.  The MDOH shall limit the number of medical cannabis manufacturer licenses granted in the state to no more than four (4) licenses.  All state-funded public universities shall have the right of first refusal to be licensed as a manufacturer, either separately or jointly.  If none of these universities exercise this option, the licenses shall be awarded pursuant to the requirements provided for in subsection (5) of this section.

     (2)  Before September 1, 2022, any state-funded public university intending to be licensed as a manufacturer shall provide written notice to the MDOH of its intent to be licensed, either separately or jointly.  Each university shall thereafter complete an application to be licensed as a medical cannabis manufacturer.

     (3)  A state-funded public university may conduct research on cannabis for medical use if the university is licensed as a manufacturer facility under this section.  Effective January 1, 2023, and annually thereafter, any state-funded public university licensed as a medical cannabis manufacturer shall submit a report to the Senate Public Health and Welfare Committee, the House Public Health and Human Services Committee and the Board of Trustees of State Institutions of Higher Learning to include data and outcomes of the research conducted under this subsection, employment statistics, audit results and medical cannabis sale results.  Any state-funded public university licensed as a medical cannabis manufacturer shall use any profit obtained from the sale of medical cannabis to offset its operating expenses.

     (4)  The license shall be limited to four (4) geographic locations as provided for in rule by the MDOH.  The geographic location shall be a public record subject to disclosure under Section 25-61-1 et seq.  The licensee shall permit inspection of the facility by any elected member of the Mississippi Legislature upon request after receipt of reasonable notice.

     (5)  (a)  If fewer than four (4) of the universities exercise the option described in subsection (1) of this section, the MDOH may award any of the remaining licenses pursuant to the following requirements:

               (i)  The technical expertise of the manufacturer in cultivating medical cannabis into an acceptable delivery method;

               (ii)  The qualifications of the manufacturer's employees;

               (iii)  The long-term financial stability of the manufacturer;

               (iv)  The ability to provide appropriate security measures on the premises of the manufacturer;

               (v)  Whether the manufacturer has demonstrated an ability to meet the medical cannabis production demands of the state.

          (b)  The licenses awarded under this subsection shall not exceed five (5) years.

          (c)  Any contract, memorandum of understanding, or cooperative endeavor agreement entered into pursuant to this section shall be a public record subject to disclosure under Section 25-61-1 et seq.

          (d)  Any contract, memorandum of understanding, or cooperative endeavor agreement entered into for services for the cultivation or processing in any way of cannabis pursuant to this section shall be a public record subject to disclosure under Section 25-61-1 et seq.

          (e)  No person or entity licensed under this subsection shall subcontract for services for the cultivation or processing in any way of cannabis if the subcontractor, or any of the service providers in the chain of subcontractors, is owned wholly or in part by any state employee or member of a state employee's immediate family, including, but not limited to, any legislator, statewide public official, university or community or technical college employee.

          (f)  No business entity licensed under this subsection shall be owned wholly or in part by any state employee or member of a state employee's immediate family, including, but not limited to, any legislator, statewide public official, university or community or technical college employee.

          (g)  Any applicant for the license awarded under this subsection shall include proof of the financial capability of the applicant to operate a medical cannabis production facility, including, but not limited to, a net worth of not less than One Million Dollars ($1,000,000.00).

          (h)  Any entity licensed under this subsection and any subcontractor of an entity licensed under this subsection shall only employ citizens of the United States who have valid social security numbers and pass a background check performed by the MDOH.

     (6)  No person or entity licensed under this section shall give or receive anything of value in connection with any contract, memorandum of understanding or cooperative endeavor agreement executed pursuant to this section except the value that is expressed in the contract, memorandum of understanding or cooperative endeavor agreement.

     (7)  (a)  The MDOH shall collect the following information from each licensee:

               (i)  The amount of gross cannabis produced by the licensee during each calendar year;

               (ii)  The details of all production costs, including, but not limited to, seed, fertilizer, labor, advisory services, construction and irrigation;

               (iii)  The details of any items or services for which the licensee subcontracted and the costs of each subcontractor directly or indirectly working for the contractor;

               (iv)  The amount of therapeutic chemicals produced resulting from the cannabis grown pursuant to this section.

               (v)  The amounts paid each year to the licensee related to the licensee's production of medical cannabis pursuant to this section.

               (vi)  The amount of medical cannabis distributed to each specialty pharmacy licensed to dispense medical cannabis in this state during each calendar year.

          (b)  The MDOH shall provide the information collected under this subsection for the previous calendar year in the form of a written report to the Legislature no later than February first of each year.  The department shall also make a copy of the report required by this subsection available to the public on the Internet.

     (8)  The MDOH shall perform the following:

          (a)  Establish and collect an annual license fee of One Hundred Thousand Dollars ($100,000.00) from each manufacturer and an annual fee from each qualified patient of One Hundred Dollars ($100.00) for administrative and inspection costs; and

          (b)  Collect a nonrefundable application fee of Ten Thousand Dollars ($10,000.00) from each applicant applying to be a manufacturer and Five Thousand Dollars ($5,000.00) from each applicant applying to be a specialty pharmacy.

     (9)  A manufacturer may operate only four (4) locations where all cultivation, harvesting, manufacturing, packaging and processing shall be conducted.  All cultivation, harvesting, manufacturing, packaging and processing by a manufacturer shall be conducted in an enclosed, locked facility at a physical address provided to the MDOH during the application process.  A manufacturer must process and prepare any medical cannabis plant material into a form allowable according to this chapter before distribution to a specialty pharmacy.

     (10)  A medical cannabis manufacturer shall contract with a laboratory, subject to the MDOH's approval of the laboratory and any additional requirements set by the MDOH, for purposes of testing medical cannabis manufactured by the medical cannabis manufacturer as to content, contamination and consistency to verify that the medical cannabis meets the requirements of this chapter and any requirements set by the MDOH.  The cost of laboratory testing shall be paid by the manufacturer.  The MDOH shall implement a recall process for medical cannabis that manufacturers shall follow.  The MDOH may require manufacturers to test their products at laboratories on a quarterly basis.

     (11)  The operating documents of a manufacturer shall include:

          (a)  Procedures for the oversight of the manufacturer and procedures to ensure accurate record keeping; and

          (b)  Procedures for the implementation of appropriate security measures to deter and prevent the theft of medical cannabis and unauthorized entrance into areas containing medical cannabis.

     (12)  A manufacturer shall implement security requirements, including requirements for protection of each location by a fully operational security alarm system, facility access controls, perimeter intrusion detection systems, and a personnel identification system.

     (13)  A manufacturer shall not share office space with, refer patients to a health care practitioner, or have any financial relationship with a health care practitioner.

     (14)  A manufacturer shall not permit any person to consume medical cannabis on the property of the manufacturer.

     (15)  A manufacturer is subject to reasonable inspection by the MDOH.

     (16)  A medical cannabis manufacturer shall not employ any person who is under twenty-one (21) years of age or who has been convicted of a disqualifying felony offense.  An employee of a medical cannabis manufacturer must submit a completed criminal history records check consent form, a full set of classifiable fingerprints, and the required fees for submission to the MDOH before an employee may begin working with the manufacturer.  The MDOH shall conduct a criminal history records check of each employee of the manufacturer.

     (17)  A manufacturer shall not operate in any location, whether for distribution or cultivation, harvesting, manufacturing, packaging or processing, within one thousand five hundred (1,500) feet of a public school, private school or child care facility existing before the date of the manufacturer's registration with the MDOH.

     (18)  A manufacturer shall comply with reasonable restrictions set by the MDOH relating to signage, marketing, display, billboards, mobile advertising and advertising of medical cannabis.  A manufacturer shall not advertise on billboards or on motor vehicles.  The MDOH shall post on its website all advertising restrictions applicable to manufacturers.  The MDOH shall include these restrictions on the application for a medical cannabis manufacturer license.

     (19)  A manufacturer shall require any employee of the manufacturer who is transporting medical cannabis or medical cannabis products to a specialty pharmacy to carry identification showing that the person is an employee of the manufacturer.

     SECTION 6.  Specialty pharmacies.  (1)  The State Board of Pharmacy shall develop an annual, nontransferable specialty license for a pharmacy to dispense recommended medical cannabis.  The board shall limit the number of such licenses granted in the state to no more than ten (10) licenses.  Each specialty pharmacy shall be located based on geographical need throughout the state to improve patient access.  The board shall collect the application fee of Five Thousand Dollars ($5,000.00) and the license fee of Twenty-five Thousand Dollars ($25,000.00).

     (2)  A manufacturer may operate two (2) specialty pharmacies which shall be licensed by the board.  The board may license no more than ten (10) specialty pharmacies regardless of whether the pharmacies are operated by licensed manufacturers.  An applicant shall disclose the proposed location for the specialty pharmacy to the board during the application process.  A licensed manufacturer shall not conduct any cultivation, harvesting, manufacturing, packaging or processing at a specialty pharmacy location.

     (3)  A specialty pharmacy may dispense medical cannabis and medical cannabis products but may not dispense cannabis in a form other than those forms allowed by this chapter.  

     (4)  The State Board of Pharmacy and MDOH shall develop the rules and regulations regarding the extraction, processing and production of recommended medical cannabis, along with following the standards established in this chapter.  The rules and regulations shall require as a minimum standard that the extraction and refining process produce pharmaceutical-grade products.

     (5)  A health care practitioner and a pharmacist at a specialty pharmacy shall review the patient's information in the database of the Prescription Monitoring Program before recommending or dispensing medical cannabis, as applicable.  Pharmacists shall enter into the patient registry all pertinent patient information, including, but not limited to, dosage dispensed, date, location and date of expiration.  A pharmacist shall counsel a qualified patient about the recommended medical cannabis before dispensing it to the patient.

     (6)  A specialty pharmacy shall require that employees licensed as pharmacists be the only employees to distribute the medical cannabis to a patient.

     (7)  Before distribution of any medical cannabis, the specialty pharmacy shall:

          (a)  Verify that the specialty pharmacy has received the registry verification from the MDOH for that individual patient;

          (b)  Verify that the person requesting the distribution of medical cannabis is the patient, the patient's registered designated caregiver, or the patient's parent or legal guardian listed in the registry verification;

          (c)  Assign a tracking number to any medical cannabis distributed from the specialty pharmacy;

          (d)  Ensure that any employee of the specialty pharmacy licensed as a pharmacist has consulted with the patient to determine the proper dosage for the individual patient after reviewing the ranges of chemical compositions of the medical cannabis and the ranges of proper dosages as set by this chapter and reported by the MDOH;

          (e)  Properly package medical cannabis in compliance with the United States Poison Prevention Packing Act regarding child resistant packaging and exemptions for packaging for elderly patients, and label distributed medical cannabis with a list of all active ingredients and individually identifying information, including:

               (i)  The patient's name and date of birth;

               (ii)  The name and date of birth of the patient's registered designated caregiver or, if listed on the registry verification, the name of the patient's parent or legal guardian, if applicable;

               (iii)  The patient's registry identification number;

               (iv)  The chemical composition of the medical cannabis; and

               (v)  The dosage; and

          (f)  Ensure that the medical cannabis distributed contains a maximum of a thirty-day supply of the dosage determined for that patient.

     (8)  A specialty pharmacy shall implement security requirements, including requirements for protection of each location by a fully operational security alarm system, facility access controls, perimeter intrusion detection systems, and a personnel identification system.

     (9)  A specialty pharmacy shall not share office space with, refer patients to a health care practitioner, or have any financial relationship with a health care practitioner.

     (10)  A specialty pharmacy shall not permit any person to consume medical cannabis on the property of the pharmacy.

     (11)  A specialty pharmacy is subject to reasonable inspection by the MDOH and the State Board of Pharmacy.

     (12)  A specialty pharmacy shall not employ any person who is under twenty-one (21) years of age or who has been convicted of a disqualifying felony offense.  An employee of a specialty pharmacy must submit a completed criminal history records check consent form, a full set of classifiable fingerprints, and the required fees for submission to the MDOH and State Board of Pharmacy before an employee may begin working with the specialty pharmacy.  The MDOH and the State Board of Pharmacy shall conduct a criminal history records check of each employee of the specialty pharmacy.

     (13)  A specialty pharmacy shall not operate in any location within one thousand five hundred (1,500) feet of a public school, private school or child care facility existing before the date of the specialty pharmacy's registration with the State Board of Pharmacy.

     (14)  A specialty pharmacy shall comply with reasonable restrictions set by the State Board of Pharmacy relating to signage, marketing, display, billboards, mobile advertising and advertising of medical cannabis.  A specialty pharmacy shall not advertise on billboards or on motor vehicles.  The board shall post on its website all advertising restrictions applicable to specialty pharmacies.  The board shall include these restrictions on the application for a specialty pharmacy license.

     (15)  No person or entity licensed under this section shall subcontract for services for the dispensing of medical cannabis, if the subcontractor, or any of the service providers in the chain of subcontractors, is owned wholly or in part by any state employee or member of a state employee's immediate family, including, but not limited to, any legislator, statewide public official, university or community or technical college employee.

     (16)  No business entity licensed under this section shall be owned wholly or in part by any state employee or member of a state employee's immediate family, including, but not limited to, any legislator, statewide public official, university or community or technical college employee.

     SECTION 7.  Patient registry.  (1)  In order to have, use and maintain a reliable system to track all aspects of patient and caregiver qualification, the MDOH shall do the following:

          (a)  Establish and administer an integrated, electronic patient and caregiver registry, known as the "Mississippi Medical Cannabis Patient Registry System," that does all of the following:

               (i)  Receives and records physician certifications;              (ii)  Receives and tracks qualified patient  registrations and issuance of medical cannabis cards;

               (iii)  Receives and tracks designated caregiver registrations and issuance of medical cannabis cards;

               (iv)  Includes in the patient registry database for each registered qualified patient the name of the qualified patient and the patient's designated caregiver, if applicable, the patient's registered certifying physician, the respective  qualifying medical condition or conditions, the recommended daily dosage and type of medical cannabis, and any other information the MDOH, by rule, deems relevant;

               (v)  Verifies that a medical cannabis card is current and valid and has not been suspended, revoked or denied;

               (vi)  Tracks purchases of medical cannabis at specialty pharmacies by date, time, amount and type.

               (vii)  Determines whether a particular sale of medical cannabis transaction exceeds the permissible limit.

               (viii)  Tracks medical cannabis cards that are denied, revoked or suspended;

               (ix)  Interfaces as necessary with the statewide seed-to-sale tracking system established under this chapter;

               (x)  Tracks purchases of medical cannabis by specialty pharmacies from medical cannabis manufacturers by date, time, amount and type; and

               (xi)  Provides access as further required in subsection (2) of this section.

     (2)  The patient registry shall be accessible to the following:

          (a)  State and local law enforcement agencies, provided that the database may only be accessed upon probable cause or reasonable suspicion of a violation of a controlled substance law or of driving under the influence, and access is strictly limited to information that is necessary to verify that an individual is registered and possesses a valid and current medical cannabis card and, if appropriate, to verify that the amount and type of product in the individual's possession complies with the daily dosage limit and type of medical cannabis recommended; and

          (b)  Health care practitioners licensed to prescribe prescription drugs.

     (3)  The MDOH shall monitor patient registrations in the patient registry for practices that could facilitate unlawful diversion or misuse of cannabis and shall recommend disciplinary action as appropriate.

     (4)  Once certified, a patient and, if applicable, the patient's designated caregiver, shall register in the patient registry.  The MDOH shall develop the application and renewal process for patient and designated caregiver registration, that shall include, but not be limited to, an application form, relevant information that must be included on the form, any additional requirements for eligibility that the MDOH deems necessary, and an application fee not to exceed One Hundred Dollars ($100.00).

     (5)  The MDOH shall develop a patient application for enrollment into the registry program.  The application shall be available to the patient and given to registered health care practitioners.  The application must include:

          (a)  The name, mailing address, recent photograph of the patient and date of birth of the patient;

          (b)  The name, mailing address and telephone number of the patient's health care practitioner;

          (c)  The name, mailing address, date of birth and recent photograph of the patient's designated caregiver, if any, or the patient's parent or legal guardian if the parent or legal guardian will be acting as a caregiver; and

          (d)  A copy of the certification from the patient's health care practitioner that is dated within ninety (90) days before submitting the application that certifies that the patient has been diagnosed with a qualifying medical condition, and, if applicable, that, in the health care practitioner's medical opinion, the patient is developmentally or physically disabled and, as a result of that disability, the patient is unable to self-administer medication or acquire medical cannabis from a specialty pharmacy.

     (6)  The MDOH or an employee of the MDOH or any other state agency shall not be held civilly or criminally liable for any injury, loss of property, personal injury or death caused by an act or omission while acting within the scope of office or employment while administering the medical cannabis program.  

     (7)  The MDOH shall develop a disclosure form and require, as a condition of registration in the program, all patients to sign a copy of the disclosure that includes a statement listing subsection (6) of this section.  

     (8)  If the qualified patient or designated caregiver meets the criteria for registration, the MDOH shall place the patient or caregiver on the patient registry and issue the patient or designated caregiver a medical cannabis card.  The MDOH shall determine the criteria for revoking or suspending a medical cannabis card.  Medical cannabis cards shall be resistant to counterfeiting and tampering and, at a minimum, shall include all of the following:

          (a)  The name, address and date of birth of the qualified patient or caregiver, as applicable;

          (b)  A photograph of the qualified patient or caregiver, as applicable;

          (c)  Identification of the cardholder as a qualified patient or a caregiver;

          (d)  The expiration date, as determined by MDOH rule; and

          (e)  The following statement:  "This card is only valid in the State of Mississippi."

     (9)  Once a patient or designated caregiver is registered and issued a medical cannabis card, he or she is qualified to acquire, possess or use medical cannabis, as applicable.

     (10)  If a registered qualified patient or registered caregiver loses his or her medical cannabis card, he or she shall notify the MDOH within ten (10) days of becoming aware the card is lost or stolen.  The MDOH, by rule, shall determine the process and fee for replacing a lost or stolen card, including a process for invalidating the lost or stolen card.

     (11)  The MDOH shall adopt rules to implement this section and may impose civil penalties for violations of this section.

     SECTION 8.  Limitations.  (1)  This chapter shall not be construed to do any of the following:

          (a)  Require an insurer, organization for managed care, health benefit plan or any individual or entity providing coverage for a medical or health care service to pay for or to reimburse any other individual or entity for costs associated with the use of medical cannabis;

          (b)  Require any employer to permit, accommodate, or allow the use of medical cannabis or to modify any job or working conditions of any employee who engages in the use of medical cannabis or for any reason seeks to engage in the use of medical cannabis;

          (c)  Prohibit any employer from refusing to hire, discharging, disciplining or otherwise taking an adverse employment action against an individual with respect to hiring, discharging, tenure, terms, conditions or privileges of employment as a result, in whole or in part, of that individual's use of medical cannabis, regardless of the individual's impairment or lack of impairment resulting from the use of medical cannabis;

          (d)  Prohibit or limit the ability of any employer from establishing or enforcing a drug-testing policy, including, but not limited to, a policy that prohibits the use of medical cannabis in the workplace or from implementing a drug-free workforce program;

          (e)  Prohibit or limit any employer from adopting an employment policy requiring its employees to notify the employer if an employee possesses a medical cannabis card;

          (f)  Interfere with, impair or impede any federal restrictions on employment, including, but not limited to, regulations adopted by the United States Department of Transportation in Title 49, Code of Federal Regulations;

          (g)  Permit, authorize or establish any individual's right to begin or undertake any legal action against an employer for refusing to hire, discharging, disciplining or otherwise taking an adverse employment action against an individual with respect to hiring, discharging, tenure, terms, conditions or privileges of employment due to the individual's use of medical cannabis;

          (h)  Require a government medical assistance program, employer, property and casualty insurer, or private health insurer to reimburse an individual for costs associated with the use of medical cannabis;

          (i)  Affect, alter or otherwise impact the workers' compensation premium discount available to employers who establish a drug-free workplace policy as provided for in Section 71-3-207;

          (j)  Affect, alter or otherwise impact an employer's right to deny, or establish legal defenses to, the payment of workers' compensation benefits to an employee on the basis of a positive drug test or refusal to submit to or cooperate with a drug test, as provided under Section 71-3-121; or

          (k)  Affect, alter or supersede any obligation or condition imposed on a parolee, probationer, or an individual participating in a pretrial diversion program or other court-ordered substance abuse rehabilitation program.

     (2)  This chapter does not authorize any individual to engage in, and does not prevent the imposition of any civil, criminal or other penalties for engaging in, the following conduct:

          (a)  Undertaking any task under the influence of medical cannabis that would constitute negligence or professional malpractice;

          (b)  Possessing or engaging in the use of medical cannabis:

               (i)  On a school bus or van;

               (ii)  On the grounds of any preschool, primary or secondary school;

               (iii)  In any correctional facility;

               (iv)  On the grounds of any child care facility or home day care;

               (v)  On any form of public transportation; or

               (vi)  In any public place, including, but not limited to, any indoor or outdoor area used by or open to the general public or as a place of employment, parks, indoor or outdoor arenas and playgrounds.

     (3)  An individual who is discharged from employment

because of that individual's use of medical cannabis, or

refusal to submit to or cooperate with a drug test, shall be

legally conclusively presumed to have been discharged for

misconduct.

     (4)  A qualifying patient shall not use medical cannabis while driving a motor vehicle or boat.  A qualifying patient shall not possess medical cannabis while driving a boat or motor vehicle unless the medical cannabis is in a sealed package.

     SECTION 9.  Agency rules and regulations.  (1)  The State Board of Pharmacy shall adopt rules relating to the dispensing of recommended cannabis for medical use.  The rules shall include, but not be limited to:

          (a)  Standards, procedures and protocols for the effective use of recommended cannabis for medical use as authorized by state law and related rules and regulations;

          (b)  Standards, procedures and protocols for the dispensing and tracking of recommended medical cannabis in Mississippi;

          (c)  Procedures and protocols to provide that no recommended medical cannabis may be dispensed from, produced from, obtained from, sold to, or transferred to a location outside of this state;

          (d)  The establishment of standards, procedures and protocols for determining the amount of usable recommended medical cannabis that is necessary to constitute an adequate supply to ensure uninterrupted availability for a period of one (1) month, including amounts for topical treatments;

          (e)  The establishment of standards, procedures and protocols to ensure that all recommended medical cannabis dispensed is consistently pharmaceutical grade;

          (f)  The establishment of standards, procedures and protocols to ensure that all recommended medical cannabis dispensed is consistently pharmaceutical grade;

          (g)  The establishment of standards and procedures for the revocation, suspension and nonrenewal of licenses;

          (h)  The establishment of other licensing, renewal and operational standards which are deemed necessary by the board;

          (i)  The establishment of standards and procedures for testing recommended medical cannabis samples for levels of tetrahydrocannabinol (THC) or other testing parameters deemed appropriate by the board;

          (j)  The establishment of health, safety and security requirements for dispensers of recommended medical cannabis;

          (k)  Licensure of specialty pharmacies of recommended medical cannabis;

          (l)  The establishment of financial requirements for applicants of medical cannabis dispensing specialty pharmacy licenses under which each applicant demonstrates the following:

               (i)  The financial capacity to operate a medical cannabis dispensing specialty pharmacy; and

               (ii)  The ability to maintain an escrow account in a financial institution headquartered in Mississippi in an amount of up to One Million Dollars ($1,000,000.00), if required by the board.

     (2)  The MDOH shall adopt rules for the issuance of certifications for registered qualifying health care practitioners to make recommendations for patients to use medical cannabis.  The rules shall include, but not be limited to, all of the following:

          (a)  Requirements for an in-person patient examination and the establishment of a practitioner-patient relationship;

          (b)  Requirements for relevant information to be included in the patient's medical record;

          (c)  Requirements for review of the patient's controlled substances prescription history in the Prescription Monitoring Program;

          (d)  Requirements for obtaining the voluntary and informed written consent from the patient to use medical cannabis, or from the patient's designated caregiver to assist the patient with the use of medical cannabis, on a form created by the MDOH and accessible at no charge on its website.  The form shall include, but not be limited to, information relating to all of the following:

               (i)  The federal and state classification of cannabis as a Schedule I controlled substance;

               (ii)  The approval and oversight status of cannabis by the Food and Drug Administration;

               (iii)  The current state of research on the efficacy of cannabis to treat the qualifying medical condition;

               (iv)  The potential for addiction;

               (v)  The potential effect that cannabis may have on a patient's coordination, motor skills and cognition, including a warning against operating heavy machinery, operating a motor vehicle or engaging in activities that require an individual to be alert or respond quickly;

               (vi)  The potential side effects of cannabis use;

               (vii)  The risks, benefits and drug interactions of cannabis;

               (viii)  A statement that the use of medical cannabis could result in termination from employment without recourse and that costs may not be covered by insurance or government programs; and

               (ix)  That the patient's de-identified health information contained in the patient's medical records, practitioner certification and patient registry may be used for research purposes or used to monitor compliance with this chapter.

     (3)  MDOH and the State Board of Pharmacy shall promulgate rules and regulations regarding the chemical composition and formulation of available medical cannabis pharmaceuticals products.  The rules and regulations shall be posted on the MDOH's website.

     SECTION 10.  Violations.  (1)  Nothing in this chapter shall preclude a local or state law enforcement agency from searching a licensee where there is probable cause to believe that a criminal law has been violated and the search is conducted in conformity with constitutional and state law.

     (2)  A manufacturer or an agent of a manufacturer who intentionally transfers medical cannabis to a person other than a registered qualified patient, designated caregiver, a registered parent or legal guardian of a registered qualified patient is guilty of a felony punishable by not more than two (2) years in the custody of the Department of Corrections or by a fine of not more than Three Thousand Dollars ($3,000.00), or both.  A person convicted under this subsection shall not continue to be affiliated with the manufacturer and shall be disqualified from further participation in the program.

     (3)  A registered qualified patient, registered caregiver or a registered parent or legal guardian of a registered qualified patient who intentionally sells or otherwise transfers medical cannabis to a person other than a registered qualified patient, designated caregiver, a registered parent or legal guardian of a registered qualified patient is guilty of a felony punishable by not more than two (2) years in the custody of the Department of Corrections or by payment of a fine of not more than Three Thousand Dollars ($3,000.00), or both.

     (4)  A person who knowingly submits false records or documentation required by the MDOH to register as a manufacturer of medical cannabis is guilty of a felony punishable by not more than two (2) years in the custody of the Department of Corrections or by payment of a fine of not more than Three Thousand Dollars ($3,000.00), or both.

     (5)  A health care practitioner who knowingly refers patients to a manufacturer or to a designated caregiver, who advertises as a manufacturer, or who recommends medical cannabis to a patient while holding a financial interest in a manufacturer is guilty of a misdemeanor punishable by imprisonment for not more than ninety (90) days in the county jail or by payment of a fine of not more than One Thousand Dollars ($1,000.00), or both, and shall not recommend medical cannabis to any other patient.

     (6)  A manufacturer shall be fined up to One Thousand Dollars ($1,000.00) for any violation of this chapter where no penalty has been specified.

     (7)  (a)  A registered qualified patient who drives or otherwise operates a motor vehicle or operates a watercraft within this state while under the influence of medical cannabis shall be guilty of a felony, fined not less than Two Thousand Dollars ($2,000.00) nor more than Five Thousand Dollars ($5,000.00), and sentenced to not more than two (2) years in the custody of the Department of Corrections.

          (b)  A patient guilty under paragraph (a) of this subsection shall forfeit his or her medical cannabis card to the MDOH.

          (c)  This penalty shall be separate from any individual punished for driving under the influence in Section 63-11-30 for operating a watercraft under the influence in Section 59-23-7.

     (8)  The penalties provided for under this section, unless otherwise stated, are in addition to any other criminal, civil or administrative penalties provided for under law, rule or regulation.

     SECTION 11.  Reports.  (1)  The MDOH shall provide annual written reports to the Legislature, with the first due no later than January 1, 2023, tracking implementations of this chapter.  The report shall be made publicly available and posted on the MDOH's website.  The report shall include all of the following:

          (a)  The number of patients applying for and receiving medical cannabis cards;

          (b)  The qualifying medical conditions identified to obtain the medical cannabis cards;

          (c)  Comments from physicians and other health care providers and from pharmacists;

          (d)  Revenues and expenses of card issuance and licensing of medical cannabis facilities;

          (e)  Relevant developments in other states' cannabis laws;

          (f)  Relevant scientific research;

          (g)  Applicable tax revenue;

          (h)  The MDOH's annual operating expenses and revenue;

          (i)  Any other information available to the MDOH that would inform public officials of how this act affects the public; and

          (j)  Any suggested legislative changes to this chapter or other state laws, including changes to reflect changes in federal law or regulation or changes based on additional medical or scientific research.

     SECTION 12.  Power to examine.  (1)  The MDOH and the State Board of Pharmacy or its designee, as applicable, may examine the business affairs and conditions of any medical cannabis manufacturer and specialty pharmacy, including, but not limited to, a review of the financing, budget, revenues, sales and pricing.

     (2)  An examination under this section may cover the medical cannabis manufacturer or specialty pharmacy's business affairs, practices and conditions including, but not limited to, a review of the financing, budgets, revenues, sales and pricing.  The MDOH or State Board of Pharmacy, as applicable, shall determine the nature and scope of each examination and in doing so, shall take into account all available relevant factors concerning the financial and business affairs, practices and conditions of the examinee.  The costs incurred by MDOH or State Board of Pharmacy in conducting an examination shall be paid for by the medical cannabis establishment or specialty pharmacy, as applicable.

     (3)  When making an examination under this section, the MDOH or State Board of Pharmacy may retain attorneys, appraisers, independent economists, independent certified public accountants or other professionals and specialists as designees.  A certified public accountant retained by the MDOH or State Board of Pharmacy shall not be the same certified public accountant providing the certified annual audit as provided for in subsection (5) of this section.

     (4)  The MDOH or State Board of Pharmacy shall make a report of an examination conducted under this section and provide a copy to the medical cannabis manufacturer or specialty pharmacy as applicable.  The MDOH or State Board of Pharmacy shall then post a copy of the report on its respective website.  All working papers, recorded information, documents and copies produced by, obtained by or disclosed to the MDOH or State Board of Pharmacy or any other person in the course of an examination, other than the information contained in any official report, shall be private data and not considered a public record subject to disclosure under Section 25-61-1 et seq.

     (5)  A medical cannabis manufacturer and specialty pharmacy shall submit the results of an annual certified financial audit to the MDOH or State Board of Pharmacy no later than May 1 of each year.  The annual audit shall be conducted by an independent certified public accountant and the costs of the audit are the responsibility of the medical cannabis manufacturer or specialty pharmacy, as applicable.  

     SECTION 13.  Adverse incidents.  (1)  The MDOH shall adopt rules to establish requirements for reporting incidents when individuals who are not authorized to possess medical cannabis under this chapter are found in possession of medical cannabis.  The rules shall identify professionals required to report, the information they are required to report and actions the reporter must take to secure the medical cannabis.

     (2)  The MDOH shall adopt rules to establish requirements for law enforcement officials and health care practitioners to report incidents involving an overdose of medical cannabis to the MDOH.

     (3)  The rules shall include the method by which the MDOH will collect and tabulate reports of unauthorized possession and overdoses.

     SECTION 14.  Local ordinance.  (1)  The MDOH and State Board of Pharmacy shall not permit a specialty pharmacy or a medical cannabis manufacturer to operate in any municipality or unincorporated area of a county unless the municipality or county has authorized the operation within its boundaries as provided in subsection (2) of this section.

     (2)  A county board of supervisors may authorize, by resolution or ordinance, the operation of specialty pharmacies and medical cannabis manufacturers within the unincorporated area of the county.  A governing authority of a municipality may authorize, by resolution or ordinance, the operation of specialty pharmacies and medical cannabis manufacturers within the corporate limits of the municipality.  The county board of supervisors or governing authority of a municipality, as applicable, shall notify the MDOH and the State Board of Pharmacy not more than seven (7) calendar days after adopting the resolution or ordinance.

     (3)  This section does not prohibit a municipality or county from adopting zoning ordinances restricting the operation of specialty pharmacies or medical cannabis manufacturers within its corporate limits, including ordinances that:

          (a)  Limit the number of specialty pharmacies;

          (b)  Limit the number of medical cannabis manufacturers; or

          (c)  Limit the hours of operation of medical cannabis manufacturers and specialty pharmacies.

     SECTION 15.  Seed-to-sale tracking system.  (1)  In order to ensure that all medical cannabis sold in the state maintains product quality to protect the health and welfare of state residents, the MDOH shall establish a statewide seed-to-sale tracking system for use as an integrated cannabis and medical cannabis tracking, inventory, and verification system.  The system must allow for interface with third-party inventory and tracking systems to provide for access by this state, licensees, and law enforcement personnel, to the extent that they need and are authorized to receive or submit the information, to comply with, enforce or administer this chapter.

     (2)  At a minimum, the system must be capable of storing and providing access to information that, in conjunction with the patient registry and with one or more third-party inventory control and tracking systems, allows all of the following:

          (a)  Retention of a record of the date, time, amount and price of each sale or transfer of medical cannabis to a registered qualified patient or registered caregiver;

          (b)  Effective seed-to-sale tracking of cannabis and medical cannabis sales and transfers among licensees and with regard to integrated facility licensees, among facilities of the licensee; and

          (c)  Receipt and integration of information from third-party inventory control and tracking systems.

     SECTION 16.  Medical cannabis taxes.  (1)  A specialty pharmacy and medical cannabis manufacturer, on forms and in a manner specified by the Commissioner of Revenue, shall collect and remit the sales tax levied in Section 27-65-17(1)(a) from the gross proceeds derived from each sale of medical cannabis.

     (2)  All taxes collected under the provisions of this section shall be deposited into the Medical Cannabis Research and Opportunity Fund provided for in Section 17 of this act.

     (3)  All administrative provisions of the sales tax law and amendments thereto, including those which fix damages, penalties and interest for nonpayment of taxes and for noncompliance with the provision of the sales tax law, and all other requirements and duties imposed upon a taxpayer, shall apply to all persons liable for taxes under the provisions of this section.  The Commissioner of Revenue shall exercise all power and authority and perform all duties with respect to taxpayers under this section as are provided in the sales tax law, except where there is a conflict, then the provisions of this section shall apply.

     SECTION 17.  Medical Cannabis Research and Opportunity Fund.  (1)  There is created a Medical Cannabis Research and Opportunity Fund in the State Treasury.  Revenue generated from the seven percent (7%) retail sales tax imposed by Section 27-65-17(1)(a) shall be deposited into the fund by the State Fiscal Officer.

     (2)  All license fees and fines collected by MDOH and the State Board of Pharmacy, as applicable, shall be deposited into the Medical Cannabis Research and Opportunity Fund.

     (3)  The monies in the Medical Cannabis Research and Opportunity Fund shall be appropriated by the Legislature and shall be allocated as follows:

          (a)  The payment of all costs incurred in the operation and administration of the medical cannabis program by MDOH and the State Board of Pharmacy, as applicable; and

          (b)  If funds remain after covering the cost in paragraph (a) of this subsection, the remaining funds shall be allocated accordingly:

               (i)  Fifty percent (50%) of the remaining funds shall be allocated to the Mississippi Resident Tuition Assistance Grant Fund; and

               (ii)  Twenty-five percent (25%) of the remaining funds shall be allocated to the Mississippi Eminent Scholars Grant Fund; and

               (iii)  Twenty-five percent (25%) of the remaining funds shall be allocated to the Mississippi Rural Physicians Scholarship Program.

     SECTION 18.  Sections 1 through 17 of this act shall be codified as a new chapter in Title 41, Mississippi Code of 1972.

     SECTION 19.  Section 25-53-5, Mississippi Code of 1972, is amended as follows:

     25-53-5.  The authority shall have the following powers, duties, and responsibilities:

          (a)  (i)  The authority shall provide for the development of plans for the efficient acquisition and utilization of computer equipment and services by all agencies of state government, and provide for their implementation.  In so doing, the authority may use the MDITS' staff, at the discretion of the executive director of the authority, or the authority may contract for the services of qualified consulting firms in the field of information technology and utilize the service of such consultants as may be necessary for such purposes.  Pursuant to Section 25-53-1, the provisions of this section shall not apply to the Department of Human Services for a period of three (3) years beginning on July 1, 2017.  Pursuant to Section 25-53-1, the provisions of this section shall not apply to the Department of Child Protection Services for a period of three (3) years beginning July 1, 2017.

              (ii)  [Repealed]

          (b)  The authority shall immediately institute procedures for carrying out the purposes of this chapter and supervise the efficient execution of the powers and duties of the office of executive director of the authority.  In the execution of its functions under this chapter, the authority shall maintain as a paramount consideration the successful internal organization and operation of the several agencies so that efficiency existing therein shall not be adversely affected or impaired.  In executing its functions in relation to the institutions of higher learning and junior colleges in the state, the authority shall take into consideration the special needs of such institutions in relation to the fields of teaching and scientific research.

          (c)  Title of whatever nature of all computer equipment now vested in any agency of the State of Mississippi is hereby vested in the authority, and no such equipment shall be disposed of in any manner except in accordance with the direction of the authority or under the provisions of such rules and regulations as may hereafter be adopted by the authority in relation thereto.

          (d)  The authority shall adopt rules, regulations, and procedures governing the acquisition of computer and telecommunications equipment and services which shall, to the fullest extent practicable, insure the maximum of competition between all manufacturers of supplies or equipment or services.  In the writing of specifications, in the making of contracts relating to the acquisition of such equipment and services, and in the performance of its other duties the authority shall provide for the maximum compatibility of all information systems hereafter installed or utilized by all state agencies and may require the use of common computer languages where necessary to accomplish the purposes of this chapter.  The authority may establish by regulation and charge reasonable fees on a nondiscriminatory basis for the furnishing to bidders of copies of bid specifications and other documents issued by the authority.

          (e)  The authority shall adopt rules and regulations governing the sharing with, or the sale or lease of information technology services to any nonstate agency or person.  Such regulations shall provide that any such sharing, sale or lease shall be restricted in that same shall be accomplished only where such services are not readily available otherwise within the state, and then only at a charge to the user not less than the prevailing rate of charge for similar services by private enterprise within this state.

          (f)  The authority may, in its discretion, establish a special technical advisory committee or committees to study and make recommendations on technology matters within the competence of the authority as the authority may see fit.  Persons serving on the Information Resource Council, its task forces, or any such technical advisory committees shall be entitled to receive their actual and necessary expenses actually incurred in the performance of such duties, together with mileage as provided by law for state employees, provided the same has been authorized by a resolution duly adopted by the authority and entered on its minutes prior to the performance of such duties.

          (g)  The authority may provide for the development and require the adoption of standardized computer programs and may provide for the dissemination of information to and the establishment of training programs for the personnel of the various information technology centers of state agencies and personnel of the agencies utilizing the services thereof.

          (h)  The authority shall adopt reasonable rules and regulations requiring the reporting to the authority through the office of executive director of such information as may be required for carrying out the purposes of this chapter and may also establish such reasonable procedures to be followed in the presentation of bills for payment under the terms of all contracts for the acquisition of computer equipment and services now or hereafter in force as may be required by the authority or by the executive director in the execution of their powers and duties.

          (i)  The authority shall require such adequate documentation of information technology procedures utilized by the various state agencies and may require the establishment of such organizational structures within state agencies relating to information technology operations as may be necessary to effectuate the purposes of this chapter.

          (j)  The authority may adopt such further reasonable rules and regulations as may be necessary to fully implement the purposes of this chapter.  All rules and regulations adopted by the authority shall be published and disseminated in readily accessible form to all affected state agencies, and to all current suppliers of computer equipment and services to the state, and to all prospective suppliers requesting the same.  Such rules and regulations shall be kept current, be periodically revised, and copies thereof shall be available at all times for inspection by the public at reasonable hours in the offices of the authority.  Whenever possible no rule, regulation or any proposed amendment to such rules and regulations shall be finally adopted or enforced until copies of the proposed rules and regulations have been furnished to all interested parties for their comment and suggestions.

          (k)  The authority shall establish rules and regulations which shall provide for the submission of all contracts proposed to be executed by the executive director for computer equipment or services to the authority for approval before final execution, and the authority may provide that such contracts involving the expenditure of less than such specified amount as may be established by the authority may be finally executed by the executive director without first obtaining such approval by the authority.

          (l)  The authority is authorized to purchase, lease, or rent computer equipment or services and to operate that equipment and use those services in providing services to one or more state agencies when in its opinion such operation will provide maximum efficiency and economy in the functions of any such agency or agencies.

          (m)  Upon the request of the governing body of a political subdivision or instrumentality, the authority shall assist the political subdivision or instrumentality in its development of plans for the efficient acquisition and utilization of computer equipment and services.  An appropriate fee shall be charged the political subdivision by the authority for such assistance.

          (n)  The authority shall adopt rules and regulations governing the protest procedures to be followed by any actual or prospective bidder, offerer or contractor who is aggrieved in connection with the solicitation or award of a contract for the acquisition of computer equipment or services.  Such rules and regulations shall prescribe the manner, time and procedure for making protests and may provide that a protest not timely filed shall be summarily denied.  The authority may require the protesting party, at the time of filing the protest, to post a bond, payable to the state, in an amount that the authority determines sufficient to cover any expense or loss incurred by the state, the authority or any state agency as a result of the protest if the protest subsequently is determined by a court of competent jurisdiction to have been filed without any substantial basis or reasonable expectation to believe that the protest was meritorious; however, in no event may the amount of the bond required exceed a reasonable estimate of the total project cost.  The authority, in its discretion, also may prohibit any prospective bidder, offerer or contractor who is a party to any litigation involving any such contract with the state, the authority or any agency of the state to participate in any other such bid, offer or contract, or to be awarded any such contract, during the pendency of the litigation.

          (o)  The authority shall make a report in writing to the Legislature each year in the month of January.  Such report shall contain a full and detailed account of the work of the authority for the preceding year as specified in Section 25-53-29(3).

     All acquisitions of computer equipment and services involving the expenditure of funds in excess of the dollar amount established in Section 31-7-13(c), or rentals or leases in excess of the dollar amount established in Section 31-7-13(c) for the term of the contract, shall be based upon competitive and open specifications, and contracts therefor shall be entered into only after advertisements for bids are published in one or more daily newspapers having a general circulation in the state not less than fourteen (14) days prior to receiving sealed bids therefor.  The authority may reserve the right to reject any or all bids, and if all bids are rejected, the authority may negotiate a contract within the limitations of the specifications so long as the terms of any such negotiated contract are equal to or better than the comparable terms submitted by the lowest and best bidder, and so long as the total cost to the State of Mississippi does not exceed the lowest bid.  If the authority accepts one (1) of such bids, it shall be that which is the lowest and best.  Through December 31, 2022, the provisions of this paragraph shall not apply to acquisitions of information technology equipment and services made by the Mississippi Department of Health for the purposes of implementing, administering and/or enforcing the provisions of the Mississippi Medical Cannabis Compassion Act.

          (p)  When applicable, the authority may procure equipment, systems and related services in accordance with the law or regulations, or both, which govern the Bureau of Purchasing of the Office of General Services or which govern the Mississippi Department of Information Technology Services procurement of telecommunications equipment, software and services.

          (q)  The authority is authorized to purchase, lease, or rent information technology and services for the purpose of establishing pilot projects to investigate emerging technologies.  These acquisitions shall be limited to new technologies and shall be limited to an amount set by annual appropriation of the Legislature.  These acquisitions shall be exempt from the advertising and bidding requirement.

          (r)  All fees collected by the Mississippi Department of Information Technology Services shall be deposited into the Mississippi Department of Information Technology Services Revolving Fund unless otherwise specified by the Legislature.

          (s)  The authority shall work closely with the council to bring about effective coordination of policies, standards and procedures relating to procurement of remote sensing and geographic information systems (GIS) resources.  In addition, the authority is responsible for development, operation and maintenance of a delivery system infrastructure for geographic information systems data.  The authority shall provide a warehouse for Mississippi's geographic information systems data.

          (t)  The authority shall manage one or more State Data Centers to provide information technology services on a cost-sharing basis.  In determining the appropriate services to be provided through the State Data Center, the authority should consider those services that:

              (i)  Result in savings to the state as a whole;

              (ii)  Improve and enhance the security and reliability of the state's information and business systems; and

               (iii)  Optimize the efficient use of the state's information technology assets, including, but not limited to, promoting partnerships with the state institutions of higher learning and community colleges to capitalize on advanced information technology resources.

          (u)  The authority shall increase federal participation in the cost of the State Data Center to the extent provided by law and its shared technology infrastructure through providing such shared services to agencies that receive federal funds.  With regard to state institutions of higher learning and community colleges, the authority may provide shared services when mutually agreeable, following a determination by both the authority and the Board of Trustees of State Institutions of Higher Learning or the Mississippi Community College Board, as the case may be, that the sharing of services is mutually beneficial.

          (v)  The authority, in its discretion, may require new or replacement agency business applications to be hosted at the State Data Center.  With regard to state institutions of higher learning and community colleges, the authority and the Board of Trustees of State Institutions of Higher Learning or the Mississippi Community College Board, as the case may be, may agree that institutions of higher learning or community colleges may utilize business applications that are hosted at the State Data Center, following a determination by both the authority and the applicable board that the hosting of those applications is mutually beneficial.  In addition, the authority may establish partnerships to capitalize on the advanced technology resources of the Board of Trustees of State Institutions of Higher Learning or the Mississippi Community College Board, following a determination by both the authority and the applicable board that such a partnership is mutually beneficial.

          (w)  The authority shall provide a periodic update regarding reform-based information technology initiatives to the Chairmen of the House and Senate Accountability, Efficiency and Transparency Committees.

     From and after July 1, 2018, the expenses of this agency shall be defrayed by appropriation from the State General Fund.  In addition, in order to receive the maximum use and benefit from information technology and services, expenses for the provision of statewide shared services that facilitate cost-effective information processing and telecommunication solutions shall be defrayed by pass-through funding and shall be deposited into the Mississippi Department of Information Technology Services Revolving Fund unless otherwise specified by the Legislature.  These funds shall only be utilized to pay the actual costs incurred by the Mississippi Department of Information Technology Services for providing these shared services to state agencies.  Furthermore, state agencies shall work in full cooperation with the Board of the Mississippi Department of Information Technology Services to identify computer equipment or services to minimize duplication, reduce costs, and improve the efficiency of providing common technology services across agency boundaries.

     SECTION 20.  Section 27-104-203, Mississippi Code of 1972, is amended as follows:

     27-104-203. * * *  (1)  From and after July 1, 2016, no state agency shall charge another state agency a fee, assessment, rent, audit fee, personnel fee or other charge for services or resources received.  The provisions of this section shall not apply (a) to grants, contracts, pass-through funds, project fees or other charges for services between state agencies and the Board of Trustees of State Institutions of Higher Learning, any public university, the Mississippi Community College Board, any public community or junior college, and the State Department of Education, nor (b) to charges for services between the Board of Trustees of State Institutions of Higher Learning, any public university, the Mississippi Community College Board, any public community or junior college, and the State Department of Education, nor (c) to federal grants, pass-through funds, cost allocation charges, surplus property charges or project fees between state agencies as approved or determined by the State Fiscal Officer, nor (d) telecommunications, data center services, and/or other information technology services that are used on an as-needed basis and those costs shall be passed through to the using agency, nor (e) to federal grants, special funds, or pass-through funds, available for payment by state agencies to the Department of Finance and Administration related to Mississippi Management and Reporting Systems (MMRS) Statewide Application charges and utilities as approved or determined by the State Fiscal Officer, nor (f) * * * [Repealed ‑ see subsection (2)] to grants, contracts, pass-through funds, project fees or charges for services between the State Department of Health and other state agencies or entities, including, but not limited to, the Board of Trustees of State Institutions of Higher Learning, any public university, the Mississippi Community College Board, any public community or junior college, and the State Department of Education, for the operation of the * * * state's medical * * * marijuana cannabis program as established by * * * Sections 288.1 through 288.10, Mississippi Constitution of 1890 the Mississippi Medical Cannabis Compassion Act.  The Board of Trustees of State Institutions of Higher Learning, any public university, the Mississippi Community College Board, any public community or junior college, and the State Department of Education shall retain the authority to charge and be charged for expenditures that they deemed nonrecurring in nature by the State Fiscal Officer.

 * * * (2)  If at any time after April 9, 2021, the Mississippi Supreme Court issues a final opinion that strikes down or otherwise holds invalid in its entirety Initiative 65, which establishes a medical marijuana program in the State of Mississippi, then paragraph (f) of subsection (1) of this section shall stand repealed on the date that the opinion is issued by the Supreme Court.

     SECTION 21.  Section 27-65-111, Mississippi Code of 1972, is amended as follows:

     27-65-111.  The exemptions from the provisions of this chapter which are not industrial, agricultural or governmental, or which do not relate to utilities or taxes, or which are not properly classified as one (1) of the exemption classifications of this chapter, shall be confined to persons or property exempted by this section or by the Constitution of the United States or the State of Mississippi.  No exemptions as now provided by any other section, except the classified exemption sections of this chapter set forth herein, shall be valid as against the tax herein levied.  Any subsequent exemption from the tax levied hereunder, except as indicated above, shall be provided by amendments to this section.

     No exemption provided in this section shall apply to taxes levied by Section 27-65-15 or 27-65-21, Mississippi Code of 1972.

     The tax levied by this chapter shall not apply to the following:

          (a)  Sales of tangible personal property and services to hospitals or infirmaries owned and operated by a corporation or association in which no part of the net earnings inures to the benefit of any private shareholder, group or individual, and which are subject to and governed by Sections 41-7-123 through 41-7-127.

     Only sales of tangible personal property or services which are ordinary and necessary to the operation of such hospitals and infirmaries are exempted from tax.

          (b)  Sales of daily or weekly newspapers, and periodicals or publications of scientific, literary or educational organizations exempt from federal income taxation under Section 501(c)(3) of the Internal Revenue Code of 1954, as it exists as of March 31, 1975, and subscription sales of all magazines.

          (c)  Sales of coffins, caskets and other materials used in the preparation of human bodies for burial.

          (d)  Sales of tangible personal property for immediate export to a foreign country.

          (e)  Sales of tangible personal property to an orphanage, old men's or ladies' home, supported wholly or in part by a religious denomination, fraternal nonprofit organization or other nonprofit organization.

          (f)  Sales of tangible personal property, labor or services taxable under Sections 27-65-17, 27-65-19 and 27-65-23, to a YMCA, YWCA, a Boys' or Girls' Club owned and operated by a corporation or association in which no part of the net earnings inures to the benefit of any private shareholder, group or individual.

          (g)  Sales to elementary and secondary grade schools, junior and senior colleges owned and operated by a corporation or association in which no part of the net earnings inures to the benefit of any private shareholder, group or individual, and which are exempt from state income taxation, provided that this exemption does not apply to sales of property or services which are not to be used in the ordinary operation of the school, or which are to be resold to the students or the public.

          (h)  The gross proceeds of retail sales and the use or consumption in this state of drugs and medicines:

              (i)  Prescribed for the treatment of a human being by a person authorized to prescribe the medicines, and dispensed or prescription filled by a registered pharmacist in accordance with law; or

              (ii)  Furnished by a licensed physician, surgeon, dentist or podiatrist to his or her own patient for treatment of the patient; or

              (iii)  Furnished by a hospital for treatment of any person pursuant to the order of a licensed physician, surgeon, dentist or podiatrist; or

              (iv)  Sold to a licensed physician, surgeon, podiatrist, dentist or hospital for the treatment of a human being; or

              (v)  Sold to this state or any political subdivision or municipal corporation thereof, for use in the treatment of a human being or furnished for the treatment of a human being by a medical facility or clinic maintained by this state or any political subdivision or municipal corporation thereof.

     "Medicines," as used in this paragraph (h), shall mean and include any substance or preparation intended for use by external or internal application to the human body in the diagnosis, cure, mitigation, treatment or prevention of disease and which is commonly recognized as a substance or preparation intended for such use; provided that "medicines" do not include any auditory, prosthetic, ophthalmic or ocular device or appliance, any dentures or parts thereof or any artificial limbs or their replacement parts, articles which are in the nature of splints, bandages, pads, compresses, supports, dressings, instruments, apparatus, contrivances, appliances, devices or other mechanical, electronic, optical or physical equipment or article or the component parts and accessories thereof, or any alcoholic beverage or any other drug or medicine not commonly referred to as a prescription drug.

     Notwithstanding the preceding sentence of this paragraph (h), "medicines" as used in this paragraph (h), shall mean and include sutures, whether or not permanently implanted, bone screws, bone pins, pacemakers and other articles permanently implanted in the human body to assist the functioning of any natural organ, artery, vein or limb and which remain or dissolve in the body.

     The exemption provided in this paragraph (h) shall not apply to medical cannabis sold in accordance with the provisions of the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder.

     "Hospital," as used in this paragraph (h), shall have the meaning ascribed to it in Section 41-9-3, Mississippi Code of 1972.

     Insulin furnished by a registered pharmacist to a person for treatment of diabetes as directed by a physician shall be deemed to be dispensed on prescription within the meaning of this paragraph (h).

          (i)  Retail sales of automobiles, trucks and truck-tractors if exported from this state within forty-eight (48) hours and registered and first used in another state.

          (j)  Sales of tangible personal property or services to the Salvation Army and the Muscular Dystrophy Association, Inc.

          (k)  From July 1, 1985, through December 31, 1992, retail sales of "alcohol-blended fuel" as such term is defined in Section 75-55-5.  The gasoline-alcohol blend or the straight alcohol eligible for this exemption shall not contain alcohol distilled outside the State of Mississippi.

          (l)  Sales of tangible personal property or services to the Institute for Technology Development.

          (m)  The gross proceeds of retail sales of food and drink for human consumption made through vending machines serviced by full-line vendors from and not connected with other taxable businesses.

          (n)  The gross proceeds of sales of motor fuel.

          (o)  Retail sales of food for human consumption purchased with food stamps issued by the United States Department of Agriculture, or other federal agency, from and after October 1, 1987, or from and after the expiration of any waiver granted pursuant to federal law, the effect of which waiver is to permit the collection by the state of tax on such retail sales of food for human consumption purchased with food stamps.

          (p)  Sales of cookies for human consumption by the Girl Scouts of America no part of the net earnings from which sales inures to the benefit of any private group or individual.

          (q)  Gifts or sales of tangible personal property or services to public or private nonprofit museums of art.

          (r)  Sales of tangible personal property or services to alumni associations of state-supported colleges or universities.

          (s)  Sales of tangible personal property or services to National Association of Junior Auxiliaries, Inc., and chapters of the National Association of Junior Auxiliaries, Inc.

          (t)  Sales of tangible personal property or services to domestic violence shelters which qualify for state funding under Sections 93-21-101 through 93-21-113.

          (u)  Sales of tangible personal property or services to the National Multiple Sclerosis Society, Mississippi Chapter.

          (v)  Retail sales of food for human consumption purchased with food instruments issued the Mississippi Band of Choctaw Indians under the Women, Infants and Children Program (WIC) funded by the United States Department of Agriculture.

          (w)  Sales of tangible personal property or services to a private company, as defined in Section 57-61-5, which is making such purchases with proceeds of bonds issued under Section 57-61-1 et seq., the Mississippi Business Investment Act.

          (x)  The gross collections from the operation of self-service, coin-operated car washing equipment and sales of the service of washing motor vehicles with portable high-pressure washing equipment on the premises of the customer.

          (y)  Sales of tangible personal property or services to the Mississippi Technology Alliance.

          (z)  Sales of tangible personal property to nonprofit organizations that provide foster care, adoption services and temporary housing for unwed mothers and their children if the organization is exempt from federal income taxation under Section 501(c)(3) of the Internal Revenue Code.

          (aa)  Sales of tangible personal property to nonprofit organizations that provide residential rehabilitation for persons with alcohol and drug dependencies if the organization is exempt from federal income taxation under Section 501(c)(3) of the Internal Revenue Code.

          (bb)  (i)  Retail sales of an article of clothing or footwear designed to be worn on or about the human body and retail sales of school supplies if the sales price of the article of clothing or footwear or school supply is less than One Hundred Dollars ($100.00) and the sale takes place during a period beginning at 12:01 a.m. on the last Friday in July and ending at 12:00 midnight the following Saturday.  This paragraph (bb) shall not apply to:

                   1.  Accessories including jewelry, handbags, luggage, umbrellas, wallets, watches, briefcases, garment bags and similar items carried on or about the human body, without regard to whether worn on the body in a manner characteristic of clothing;

                   2.  The rental of clothing or footwear; and

                   3.  Skis, swim fins, roller blades, skates and similar items worn on the foot.

              (ii)  For purposes of this paragraph (bb), "school supplies" means items that are commonly used by a student in a course of study.  The following is an all-inclusive list:

                   1.  Backpacks;

                   2.  Binder pockets;

                   3.  Binders;

                   4.  Blackboard chalk;

                   5.  Book bags;

                   6.  Calculators;

                   7.  Cellophane tape;

                    8.  Clays and glazes;

                   9.  Compasses;

                   10.  Composition books;

                   11.  Crayons;

                   12.  Dictionaries and thesauruses;

                   13.  Dividers;

                   14.  Erasers;

                   15.  Folders:  expandable, pocket, plastic and manila;

                   16.  Glue, paste and paste sticks;

                    17.  Highlighters;

                   18.  Index card boxes;

                   19.  Index cards;

                   20.  Legal pads;

                   21.  Lunch boxes;

                   22.  Markers;

                   23.  Notebooks;

                   24.  Paintbrushes for artwork;

                   25.  Paints:  acrylic, tempera and oil;

                    26.  Paper:  loose-leaf ruled notebook paper, copy paper, graph paper, tracing paper, manila paper, colored paper, poster board and construction paper;

                   27.  Pencil boxes and other school supply boxes;

                   28.  Pencil sharpeners;

                   29.  Pencils;

                    30.  Pens;

                   31.  Protractors;

                   32.  Reference books;

                   33.  Reference maps and globes;

                   34.  Rulers;

                   35.  Scissors;

                   36.  Sheet music;

                   37.  Sketch and drawing pads;

                   38.  Textbooks;

                    39.  Watercolors;

                   40.  Workbooks; and

                    41.  Writing tablets.

               (iii)  From and after January 1, 2010, the governing authorities of a municipality, for retail sales occurring within the corporate limits of the municipality, may suspend the application of the exemption provided for in this paragraph (bb) by adoption of a resolution to that effect stating the date upon which the suspension shall take effect.  A certified copy of the resolution shall be furnished to the Department of Revenue at least ninety (90) days prior to the date upon which the municipality desires such suspension to take effect.

          (cc)  The gross proceeds of sales of tangible personal property made for the sole purpose of raising funds for a school or an organization affiliated with a school.

     As used in this paragraph (cc), "school" means any public or private school that teaches courses of instruction to students in any grade from kindergarten through Grade 12.

          (dd)  Sales of durable medical equipment and home medical supplies when ordered or prescribed by a licensed physician for medical purposes of a patient.  As used in this paragraph (dd), "durable medical equipment" and "home medical supplies" mean equipment, including repair and replacement parts for the equipment or supplies listed under Title XVIII of the Social Security Act or under the state plan for medical assistance under Title XIX of the Social Security Act, prosthetics, orthotics, hearing aids, hearing devices, prescription eyeglasses, oxygen and oxygen equipment.  Payment does not have to be made, in whole or in part, by any particular person to be eligible for this exemption.  Purchases of home medical equipment and supplies by a provider of home health services or a provider of hospice services are eligible for this exemption if the purchases otherwise meet the requirements of this paragraph.

          (ee)  Sales of tangible personal property or services to Mississippi Blood Services.

          (ff)  (i)  Subject to the provisions of this paragraph (ff), retail sales of firearms, ammunition and hunting supplies if sold during the annual Mississippi Second Amendment Weekend holiday beginning at 12:01 a.m. on the last Friday in August and ending at 12:00 midnight the following Sunday.  For the purposes of this paragraph (ff), "hunting supplies" means tangible personal property used for hunting, including, and limited to, archery equipment, firearm and archery cases, firearm and archery accessories, hearing protection, holsters, belts and slings.  Hunting supplies does not include animals used for hunting.

              (ii)  This paragraph (ff) shall apply only if one or more of the following occur:

                   1.  Title to and/or possession of an eligible item is transferred from a seller to a purchaser; and/or

                   2.  A purchaser orders and pays for an eligible item and the seller accepts the order for immediate shipment, even if delivery is made after the time period provided in subparagraph (i) of this paragraph (ff), provided that the purchaser has not requested or caused the delay in shipment.

          (gg)  Sales of nonperishable food items to charitable organizations that are exempt from federal income taxation under Section 501(c)(3) of the Internal Revenue Code and operate a food bank or food pantry or food lines.

          (hh)  Sales of tangible personal property or services to the United Way of the Pine Belt Region, Inc.

          (ii)  Sales of tangible personal property or services to the Mississippi Children's Museum or any subsidiary or affiliate thereof operating a satellite or branch museum within this state.

          (jj)  Sales of tangible personal property or services to the Jackson Zoological Park.

          (kk)  Sales of tangible personal property or services to the Hattiesburg Zoo.

          (ll)  Gross proceeds from sales of food, merchandise or other concessions at an event held solely for religious or charitable purposes at livestock facilities, agriculture facilities or other facilities constructed, renovated or expanded with funds for the grant program authorized under Section 18, Chapter 530, Laws of 1995.

          (mm)  Sales of tangible personal property and services to the Diabetes Foundation of Mississippi and the Mississippi Chapter of the Juvenile Diabetes Research Foundation.

          (nn)  Sales of potting soil, mulch, or other soil amendments used in growing ornamental plants which bear no fruit of commercial value when sold to commercial plant nurseries that operate exclusively at wholesale and where no retail sales can be made.

          (oo)  Sales of tangible personal property or services to the University of Mississippi Medical Center Research Development Foundation.

          (pp)  Sales of tangible personal property or services to Keep Mississippi Beautiful, Inc., and all affiliates of Keep Mississippi Beautiful, Inc.

          (qq)  Sales of tangible personal property or services to the Friends of Children's Hospital.

          (rr)  Sales of tangible personal property or services to the Pinecrest Weekend Snackpacks for Kids located in Corinth, Mississippi.

          (ss)  Sales of hearing aids when ordered or prescribed by a licensed physician, audiologist or hearing aid specialist for the medical purposes of a patient.

          (tt)  Sales exempt under the Facilitating Business Rapid Response to State Declared Disasters Act of 2015 (Sections 27-113-1 through 27-113-9).

          (uu)  Sales of tangible personal property or services to the Junior League of Jackson.

          (vv)  Sales of tangible personal property or services to the Mississippi's Toughest Kids Foundation for use in the construction, furnishing and equipping of buildings and related facilities and infrastructure at Camp Kamassa in Copiah County, Mississippi.  This paragraph (vv) shall stand repealed on July 1, 2022.

          (ww)  Sales of tangible personal property or services to MS Gulf Coast Buddy Sports, Inc.

          (xx)  Sales of tangible personal property or services to Biloxi Lions, Inc.

          (yy)  Sales of tangible personal property or services to Lions Sight Foundation of Mississippi, Inc.

          (zz)  Sales of tangible personal property and services to the Goldring/Woldenberg Institute of Southern Jewish Life (ISJL).

     SECTION 22.  Section 33-13-520, Mississippi Code of 1972, is amended as follows:

     33-13-520.  (1)  Any person subject to this code who uses, while on duty, any controlled substance listed in the Uniform Controlled Substances Law, not legally prescribed, or is found, by a chemical analysis of such person's blood or urine, to have in his or her blood, while on duty, any controlled substance described in subsection (3), not legally prescribed, shall be punished as a court-martial may direct.

     (2)  Any person subject to this code who wrongfully uses, possesses, manufactures, distributes, imports into the customs territory of the United States, exports from the United States, or introduces into an installation, vessel, vehicle or aircraft used by or under the control of the state military forces a substance described in subsection (3) shall be punished as a court-martial may direct.

     (3)  The substances referred to in subsections (1) and (2) are the following:

          (a)  Opium, heroin, cocaine, amphetamine, lysergic acid diethylamide, methamphetamine, phencyclidine, barbituric acid, and marijuana and any compound or derivative of any such substance.  For the purposes of this paragraph (a), "marijuana" shall not include medical cannabis that is lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder.

          (b)  Any substance not specified in paragraph (a) that is listed on a schedule of controlled substance prescribed by the President for the purposes of the federal Uniform Code of Military Justice.

          (c)  Any other substance not specified in paragraph (a) or contained on a list prescribed by the President under paragraph (b) that is listed in Schedules I through V of Section 202 of the federal Controlled Substances Act (21 USCS 812).

     SECTION 23.  Section 41-29-125, Mississippi Code of 1972, is amended as follows:

     41-29-125.  (1)  The State Board of Pharmacy may promulgate rules and regulations relating to the registration and control of the manufacture, distribution and dispensing of controlled substances, including medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act, within this state and the distribution and dispensing of controlled substances into this state from an out-of-state location.

          (a)  Every person who manufactures, distributes or dispenses any controlled substance within this state or who distributes or dispenses any controlled substance into this state from an out-of-state location, or who proposes to engage in the manufacture, distribution or dispensing of any controlled substance within this state or the distribution or dispensing of any controlled substance into this state from an out-of-state location, must obtain a registration issued by the State Board of Pharmacy, the State Board of Medical Licensure, the State Board of Dental Examiners, the Mississippi Board of Nursing or the Mississippi Board of Veterinary Medicine, as appropriate, in accordance with its rules and the law of this state.  Such registration shall be obtained annually or biennially, as specified by the issuing board, and a reasonable fee may be charged by the issuing board for such registration.

          (b)  Persons registered by the State Board of Pharmacy, with the consent of the United States Drug Enforcement Administration and the State Board of Medical Licensure, the State Board of Dental Examiners, the Mississippi Board of Nursing or the Mississippi Board of Veterinary Medicine to manufacture, distribute, dispense or conduct research with controlled substances may possess, manufacture, distribute, dispense or conduct research with those substances to the extent authorized by their registration and in conformity with the other provisions of this article.

          (c)  The following persons need not register and may lawfully possess controlled substances under this article:

               ( * * *1i)  An agent or employee of any registered manufacturer, distributor or dispenser of any controlled substance if he or she is acting in the usual course of his or her business or employment;

              ( * * *2ii)  A common or contract carrier or warehouse, or an employee thereof, whose possession of any controlled substance is in the usual course of business or employment;

              ( * * *3iii)  An ultimate user or a person in possession of any controlled substance pursuant to a valid prescription or in lawful possession of a Schedule V substance as defined in Section 41-29-121.

          (d)  The State Board of Pharmacy may waive by rule the requirement for registration of certain manufacturers, distributors or dispensers if it finds it consistent with the public health and safety.

          (e)  A separate registration is required at each principal place of business or professional practice where an applicant within the state manufactures, distributes or dispenses controlled substances and for each principal place of business or professional practice located out of state from which controlled substances are distributed or dispensed into the state.

          (f)  The State Board of Pharmacy, the Mississippi Bureau of Narcotics, the State Board of Medical Licensure, the State Board of Dental Examiners, the Mississippi Board of Nursing and the Mississippi Board of Veterinary Medicine may inspect the establishment of a registrant or applicant for registration in accordance with the regulations of these agencies as approved by the board.

     (2)  Whenever a pharmacy ships, mails or delivers any Schedule II controlled substance listed in Section 41-29-115 to a private residence in this state, the pharmacy shall arrange with the entity that will actually deliver the controlled substance to a recipient in this state that the entity will:  (a) deliver the controlled substance only to a person who is eighteen (18) years of age or older; and (b) obtain the signature of that person before delivering the controlled substance.  The requirements of this subsection shall not apply to a pharmacy serving a nursing facility or to a pharmacy owned and/or operated by a hospital, nursing facility or clinic to which the general public does not have access to purchase pharmaceuticals on a retail basis.

     SECTION 24.  Section 41-29-127, Mississippi Code of 1972, is amended as follows:

     41-29-127.  (a)  The State Board of Pharmacy shall register an applicant to manufacture or distribute controlled substances included in Sections 41-29-113 through 41-29-121 and the Mississippi Medical Cannabis Compassion Act, unless it determines that the issuance of that registration would be inconsistent with the public interest.  In determining the public interest, the State Board of Pharmacy shall consider the following factors:

          (1)  Maintenance of effective controls against diversion of controlled substances into other than legitimate medical, scientific, or industrial channels;

          (2)  Compliance with applicable state and local law;

          (3)  Any convictions of the applicant under any federal and state laws relating to any controlled substance;

          (4)  Past experience in the manufacture or distribution of controlled substances and the existence in the applicant's establishment of effective controls against diversion;

          (5)  Furnishing by the applicant of false or fraudulent material in any application filed under this article;

          (6)  Suspension or revocation of the applicant's federal registration to manufacture, distribute, or dispense controlled substances as authorized by federal law; and

          (7)  Any other factors relevant to and consistent with the public health and safety. 

     (b)  Registration under subsection (a) does not entitle a registrant to manufacture and distribute controlled substances in Schedule I or II, as set out in Sections 41-29-113 and 41-29-115, other than those specified in the registration. 

     (c)  Practitioners must be registered to dispense any controlled substances or to conduct research with controlled substances in Schedules II through V, as set out in Sections 41-29-115 through 41-29-121, if they are authorized to dispense or conduct research under the law of this state.  The State Board of Pharmacy need not require separate registration under this section for practitioners engaging in research with nonnarcotic controlled substances in the said Schedules II through V where the registrant is already registered therein in another capacity.  Practitioners registered under federal law to conduct research with Schedule I substances, as set out in Section 41-29-113, may conduct research with Schedule I substances within this state upon furnishing the State Board of Health evidence of that federal registration. 

     (d)  Compliance by manufacturers and distributors with the provisions of the federal law respecting registration (excluding fees) entitles them to be registered under this article.

     SECTION 25.  Section 41-29-136, Mississippi Code of 1972, is amended as follows:

     41-29-136.  (1)  "CBD solution" means a pharmaceutical preparation consisting of processed cannabis plant extract in oil or other suitable vehicle.

     (2)  (a)  CBD solution prepared from (i) Cannabis plant extract that is provided by the National Center for Natural Products Research at the University of Mississippi under appropriate federal and state regulatory approvals, or (ii) Cannabis extract from hemp produced pursuant to Sections 69-25-201 through 69-25-221, which is prepared and tested to meet compliance with regulatory specifications, may be dispensed by the Department of Pharmacy Services at the University of Mississippi Medical Center (UMMC Pharmacy) after mixing the extract with a suitable vehicle.  The CBD solution may be prepared by the UMMC Pharmacy or by another pharmacy or laboratory in the state under appropriate federal and state regulatory approvals and registrations.

          (b)  The patient or the patient's parent, guardian or custodian must execute a hold-harmless agreement that releases from liability the state and any division, agency, institution or employee thereof involved in the research, cultivation, processing, formulating, dispensing, prescribing or administration of CBD solution obtained from entities authorized under this section to produce or possess cannabidiol for research under appropriate federal and state regulatory approvals and registrations.

          (c)  The National Center for Natural Products Research at the University of Mississippi and the Mississippi Agricultural and Forestry Experiment Station at Mississippi State University are the only entities authorized to produce cannabis plants for cannabidiol research.

          (d)  Research of CBD solution under this section must comply with the provisions of Section 41-29-125 regarding lawful possession of controlled substances, of Section 41-29-137 regarding record-keeping requirements relative to the dispensing, use or administration of controlled substances, and of Section 41-29-133 regarding inventory requirements, insofar as they are applicable.  Authorized entities may enter into public-private partnerships to facilitate research.

     (3)  (a)  In a prosecution for the unlawful possession of marijuana under the laws of this state, it is an affirmative and complete defense to prosecution that:

              (i)  The defendant suffered from a debilitating epileptic condition or related illness and the use or possession of CBD solution was pursuant to the order of a physician as authorized under this section; or

              (ii)  The defendant is the parent, guardian or custodian of an individual who suffered from a debilitating epileptic condition or related illness and the use or possession of CBD solution was pursuant to the order of a physician as authorized under this section.

          (b)  An agency of this state or a political subdivision thereof, including any law enforcement agency, may not initiate proceedings to remove a child from the home based solely upon the possession or use of CBD solution by the child or parent, guardian or custodian of the child as authorized under this section.

          (c)  An employee of the state or any division, agency, institution thereof involved in the research, cultivation, processing, formulation, dispensing, prescribing or administration of CBD solution shall not be subject to prosecution for unlawful possession, use, distribution or prescription of marijuana under the laws of this state for activities arising from or related to the use of CBD solution in the treatment of individuals diagnosed with a debilitating epileptic condition.

     (4)  This section does not apply to any of the actions that are lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations thereunder.

     ( * * *45)  This section shall be known as "Harper Grace's Law."

     ( * * *56)  This section shall stand repealed from and after July 1, 2024.

     SECTION 26.  Section 41-29-137, Mississippi Code of 1972, is amended as follows:

     41-29-137.  (a)  (1)  Except when dispensed directly by a practitioner, other than a pharmacy, to an ultimate user, no controlled substance in Schedule II, as set out in Section 41-29-115, may be dispensed without the written valid prescription of a practitioner.  A practitioner shall keep a record of all controlled substances in Schedule I, II and III administered, dispensed or professionally used by him or her otherwise than by prescription.

          (2)  In emergency situations, as defined by rule of the State Board of Pharmacy, Schedule II drugs may be dispensed upon the oral valid prescription of a practitioner, reduced promptly to writing and filed by the pharmacy.  Prescriptions shall be retained in conformity with the requirements of Section 41-29-133.  No prescription for a Schedule II substance may be refilled unless renewed by prescription issued by a licensed medical doctor.

     (b)  Except when dispensed directly by a practitioner, other than a pharmacy, to an ultimate user, a controlled substance included in Schedule III or IV, as set out in Sections 41-29-117 and 41-29-119, shall not be dispensed without a written or oral valid prescription of a practitioner.  The prescription shall not be filled or refilled more than six (6) months after the date thereof or be refilled more than five (5) times, unless renewed by the practitioner.

     (c)  A controlled substance included in Schedule V, as set out in Section 41-29-121, shall not be distributed or dispensed other than for a medical purpose.

     (d)  An optometrist certified to prescribe and use therapeutic pharmaceutical agents under Sections 73-19-153 through 73-19-165 shall be authorized to prescribe oral analgesic controlled substances in Schedule IV or V, as pertains to treatment and management of eye disease by written prescription only.

     (e)  Administration by injection of any pharmaceutical product authorized in this section is expressly prohibited except when dispensed directly by a practitioner other than a pharmacy.

     (f)  (1)  For the purposes of this article, Title 73, Chapter 21, and Title 73, Chapter 25, Mississippi Code of 1972, as it pertains to prescriptions for controlled substances, a "valid prescription" means a prescription that is issued for a legitimate medical purpose in the usual course of professional practice by:

              (A)  A practitioner who has conducted at least one (1) in-person medical evaluation of the patient, except as otherwise authorized by Section 41-29-137.1; or

              (B)  A covering practitioner.

          (2)  (A)  "In-person medical evaluation" means a medical evaluation that is conducted with the patient in the physical presence of the practitioner, without regard to whether portions of the evaluation are conducted by other health professionals.

              (B)  "Covering practitioner" means a practitioner who conducts a medical evaluation other than an in-person medical evaluation at the request of a practitioner who has conducted at least one (1) in-person medical evaluation of the patient or an evaluation of the patient through the practice of telemedicine within the previous twenty-four (24) months and who is temporarily unavailable to conduct the evaluation of the patient.

          (3)  A prescription for a controlled substance based solely on a consumer's completion of an online medical questionnaire is not a valid prescription.

          (4)  Nothing in this subsection (f) shall apply to:

              (A)  A prescription issued by a practitioner engaged in the practice of telemedicine as authorized under state or federal law; or

              (B)  The dispensing or selling of a controlled substance pursuant to practices as determined by the United States Attorney General by regulation.

     (g)  This section does not apply to any of the actions that are lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder.

     SECTION 27.  Section 41-29-139, Mississippi Code of 1972, is amended as follows:

     41-29-139.  (a)  Transfer and possession with intent to transfer.  Except as authorized by this article, it is unlawful for any person knowingly or intentionally:

          (1)  To sell, barter, transfer, manufacture, distribute, dispense or possess with intent to sell, barter, transfer, manufacture, distribute or dispense, a controlled substance; or

          (2)  To create, sell, barter, transfer, distribute, dispense or possess with intent to create, sell, barter, transfer, distribute or dispense, a counterfeit substance.

     (b)  Punishment for transfer and possession with intent to transfer.  Except as otherwise provided in Section 41-29-142, any person who violates subsection (a) of this section shall be, if convicted, sentenced as follows:

          (1)  For controlled substances classified in Schedule I or II, as set out in Sections 41-29-113 and 41-29-115, other than marijuana or synthetic cannabinoids:

              (A)  If less than two (2) grams or ten (10) dosage units, by imprisonment for not more than eight (8) years or a fine of not more than Fifty Thousand Dollars ($50,000.00), or both.

              (B)  If two (2) or more grams or ten (10) or more dosage units, but less than ten (10) grams or twenty (20) dosage units, by imprisonment for not less than three (3) years nor more than twenty (20) years or a fine of not more than Two Hundred Fifty Thousand Dollars ($250,000.00), or both.

              (C)  If ten (10) or more grams or twenty (20) or more dosage units, but less than thirty (30) grams or forty (40) dosage units, by imprisonment for not less than five (5) years nor more than thirty (30) years or a fine of not more than Five Hundred Thousand Dollars ($500,000.00), or both.

          (2)  (A)  For marijuana:

                   1.  If thirty (30) grams or less, by imprisonment for not more than three (3) years or a fine of not more than Three Thousand Dollars ($3,000.00), or both;

                   2.  If more than thirty (30) grams but less than two hundred fifty (250) grams, by imprisonment for not more than five (5) years or a fine of not more than Five Thousand Dollars ($5,000.00), or both;

                   3.  If two hundred fifty (250) or more grams but less than five hundred (500) grams, by imprisonment for not less than three (3) years nor more than ten (10) years or a fine of not more than Fifteen Thousand Dollars ($15,000.00), or both;

                   4.  If five hundred (500) or more grams but less than one (1) kilogram, by imprisonment for not less than five (5) years nor more than twenty (20) years or a fine of not more than Twenty Thousand Dollars ($20,000.00), or both.

              (B)  For synthetic cannabinoids:

                   1.  If ten (10) grams or less, by imprisonment for not more than three (3) years or a fine of not more than Three Thousand Dollars ($3,000.00), or both;

                   2.  If more than ten (10) grams but less than twenty (20) grams, by imprisonment for not more than five (5) years or a fine of not more than Five Thousand Dollars ($5,000.00), or both;

                   3.  If twenty (20) or more grams but less than forty (40) grams, by imprisonment for not less than three (3) years nor more than ten (10) years or a fine of not more than Fifteen Thousand Dollars ($15,000.00), or both;

                   4.  If forty (40) or more grams but less than two hundred (200) grams, by imprisonment for not less than five (5) years nor more than twenty (20) years or a fine of not more than Twenty Thousand Dollars ($20,000.00), or both.

          (3)  For controlled substances classified in Schedules III and IV, as set out in Sections 41-29-117 and 41-29-119:

              (A)  If less than two (2) grams or ten (10) dosage units, by imprisonment for not more than five (5) years or a fine of not more than Five Thousand Dollars ($5,000.00), or both;

              (B)  If two (2) or more grams or ten (10) or more dosage units, but less than ten (10) grams or twenty (20) dosage units, by imprisonment for not more than eight (8) years or a fine of not more than Fifty Thousand Dollars ($50,000.00), or both;

              (C)  If ten (10) or more grams or twenty (20) or more dosage units, but less than thirty (30) grams or forty (40) dosage units, by imprisonment for not more than fifteen (15) years or a fine of not more than One Hundred Thousand Dollars ($100,000.00), or both;

              (D)  If thirty (30) or more grams or forty (40) or more dosage units, but less than five hundred (500) grams or two thousand five hundred (2,500) dosage units, by imprisonment for not more than twenty (20) years or a fine of not more than Two Hundred Fifty Thousand Dollars ($250,000.00), or both.

          (4)  For controlled substances classified in Schedule V, as set out in Section 41-29-121:

              (A)  If less than two (2) grams or ten (10) dosage units, by imprisonment for not more than one (1) year or a fine of not more than Five Thousand Dollars ($5,000.00), or both;

              (B)  If two (2) or more grams or ten (10) or more dosage units, but less than ten (10) grams or twenty (20) dosage units, by imprisonment for not more than five (5) years or a fine of not more than Ten Thousand Dollars ($10,000.00), or both;

              (C)  If ten (10) or more grams or twenty (20) or more dosage units, but less than thirty (30) grams or forty (40) dosage units, by imprisonment for not more than ten (10) years or a fine of not more than Twenty Thousand Dollars ($20,000.00), or both;

              (D)  For thirty (30) or more grams or forty (40) or more dosage units, but less than five hundred (500) grams or two thousand five hundred (2,500) dosage units, by imprisonment for not more than fifteen (15) years or a fine of not more than Fifty Thousand Dollars ($50,000.00), or both.

     (c)  Simple possession.  Except as otherwise provided under subsection (i) of this section for actions that are lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder, it is unlawful for any person knowingly or intentionally to possess any controlled substance unless the substance was obtained directly from, or pursuant to, a valid prescription or order of a practitioner while acting in the course of his or her professional practice, or except as otherwise authorized by this article.  The penalties for any violation of this subsection (c) with respect to a controlled substance classified in Schedules I, II, III, IV or V, as set out in Section 41-29-113, 41-29-115, 41-29-117, 41-29-119 or 41-29-121, including marijuana or synthetic cannabinoids, shall be based on dosage unit as defined herein or the weight of the controlled substance as set forth herein as appropriate:

     "Dosage unit (d.u.)" means a tablet or capsule, or in the case of a liquid solution, one (1) milliliter.  In the case of lysergic acid diethylamide (LSD) the term, "dosage unit" means a stamp, square, dot, microdot, tablet or capsule of a controlled substance.

     For any controlled substance that does not fall within the definition of the term "dosage unit," the penalties shall be based upon the weight of the controlled substance.

     The weight set forth refers to the entire weight of any mixture or substance containing a detectable amount of the controlled substance.

     If a mixture or substance contains more than one (1) controlled substance, the weight of the mixture or substance is assigned to the controlled substance that results in the greater punishment.

      A person shall be charged and sentenced as follows for a violation of this subsection with respect to:

          (1)  A controlled substance classified in Schedule I or II, except marijuana and synthetic cannabinoids:

               (A)  If less than one-tenth (0.1) gram or two (2) dosage units, the violation is a misdemeanor and punishable by imprisonment for not more than one (1) year or a fine of not more than One Thousand Dollars ($1,000.00), or both.

              (B)  If one-tenth (0.1) gram or more or two (2) or more dosage units, but less than two (2) grams or ten (10) dosage units, by imprisonment for not more than three (3) years or a fine of not more than Fifty Thousand Dollars ($50,000.00), or both.

              (C)  If two (2) or more grams or ten (10) or more dosage units, but less than ten (10) grams or twenty (20) dosage units, by imprisonment for not more than eight (8) years or a fine of not more than Two Hundred Fifty Thousand Dollars ($250,000.00), or both.

              (D)  If ten (10) or more grams or twenty (20) or more dosage units, but less than thirty (30) grams or forty (40) dosage units, by imprisonment for not less than three (3) years nor more than twenty (20) years or a fine of not more than Five Hundred Thousand Dollars ($500,000.00), or both.

          (2)  (A)  Marijuana and synthetic cannabinoids:

                   1.  If thirty (30) grams or less of marijuana or ten (10) grams or less of synthetic cannabinoids, by a fine of not less than One Hundred Dollars ($100.00) nor more than Two Hundred Fifty Dollars ($250.00).  The provisions of this paragraph (2)(A) may be enforceable by summons if the offender provides proof of identity satisfactory to the arresting officer and gives written promise to appear in court satisfactory to the arresting officer, as directed by the summons.  A second conviction under this section within two (2) years is a misdemeanor punishable by a fine of Two Hundred Fifty Dollars ($250.00), not more than sixty (60) days in the county jail, and mandatory participation in a drug education program approved by the Division of Alcohol and Drug Abuse of the State Department of Mental Health, unless the court enters a written finding that a drug education program is inappropriate.  A third or subsequent conviction under this paragraph (2)(A) within two (2) years is a misdemeanor punishable by a fine of not less than Two Hundred Fifty Dollars ($250.00) nor more than One Thousand Dollars ($1,000.00) and confinement for not more than six (6) months in the county jail.

     Upon a first or second conviction under this paragraph (2)(A), the courts shall forward a report of the conviction to the Mississippi Bureau of Narcotics which shall make and maintain a private, nonpublic record for a period not to exceed two (2) years from the date of conviction.  The private, nonpublic record shall be solely for the use of the courts in determining the penalties which attach upon conviction under this paragraph (2)(A) and shall not constitute a criminal record for the purpose of private or administrative inquiry and the record of each conviction shall be expunged at the end of the period of two (2) years following the date of such conviction;

                   2.  Additionally, a person who is the operator of a motor vehicle, who possesses on his or her person or knowingly keeps or allows to be kept in a motor vehicle within the area of the vehicle normally occupied by the driver or passengers, more than one (1) gram, but not more than thirty (30) grams of marijuana or not more than ten (10) grams of synthetic cannabinoids is guilty of a misdemeanor and, upon conviction, may be fined not more than One Thousand Dollars ($1,000.00) or confined for not more than ninety (90) days in the county jail, or both.  For the purposes of this subsection, such area of the vehicle shall not include the trunk of the motor vehicle or the areas not normally occupied by the driver or passengers if the vehicle is not equipped with a trunk.  A utility or glove compartment shall be deemed to be within the area occupied by the driver and passengers * * *;.

              (B)  Marijuana:

                   1.  If more than thirty (30) grams but less than two hundred fifty (250) grams, by a fine of not more than One Thousand Dollars ($1,000.00), or confinement in the county jail for not more than one (1) year, or both; or by a fine of not more than Three Thousand Dollars ($3,000.00), or imprisonment in the custody of the Department of Corrections for not more than three (3) years, or both;

                   2.  If two hundred fifty (250) or more grams but less than five hundred (500) grams, by imprisonment for not less than two (2) years nor more than eight (8) years or by a fine of not more than Fifty Thousand Dollars ($50,000.00), or both;

                   3.  If five hundred (500) or more grams but less than one (1) kilogram, by imprisonment for not less than four (4) years nor more than sixteen (16) years or a fine of not more than Two Hundred Fifty Thousand Dollars ($250,000.00), or both;

                   4.  If one (1) kilogram or more but less than five (5) kilograms, by imprisonment for not less than six (6) years nor more than twenty-four (24) years or a fine of not more than Five Hundred Thousand Dollars ($500,000.00), or both;

                   5.  If five (5) kilograms or more, by imprisonment for not less than ten (10) years nor more than thirty (30) years or a fine of not more than One Million Dollars ($1,000,000.00), or both.

              (C)  Synthetic cannabinoids:

                   1.  If more than ten (10) grams but less than twenty (20) grams, by a fine of not more than One Thousand Dollars ($1,000.00), or confinement in the county jail for not more than one (1) year, or both; or by a fine of not more than Three Thousand Dollars ($3,000.00), or imprisonment in the custody of the Department of Corrections for not more than three (3) years, or both;

                   2.  If twenty (20) or more grams but less than forty (40) grams, by imprisonment for not less than two (2) years nor more than eight (8) years or by a fine of not more than Fifty Thousand Dollars ($50,000.00), or both;

                   3.  If forty (40) or more grams but less than two hundred (200) grams, by imprisonment for not less than four (4) years nor more than sixteen (16) years or a fine of not more than Two Hundred Fifty Thousand Dollars ($250,000.00), or both;

                   4.  If two hundred (200) or more grams, by imprisonment for not less than six (6) years nor more than twenty-four (24) years or a fine of not more than Five Hundred Thousand Dollars ($500,000.00), or both.

          (3)  A controlled substance classified in Schedule III, IV or V as set out in Sections 41-29-117 through 41-29-121, upon conviction, may be punished as follows:

              (A)  If less than fifty (50) grams or less than one hundred (100) dosage units, the offense is a misdemeanor and punishable by not more than one (1) year or a fine of not more than One Thousand Dollars ($1,000.00), or both.

              (B)  If fifty (50) or more grams or one hundred (100) or more dosage units, but less than one hundred fifty (150) grams or five hundred (500) dosage units, by imprisonment for not less than one (1) year nor more than four (4) years or a fine of not more than Ten Thousand Dollars ($10,000.00), or both.

              (C)  If one hundred fifty (150) or more grams or five hundred (500) or more dosage units, but less than three hundred (300) grams or one thousand (1,000) dosage units, by imprisonment for not less than two (2) years nor more than eight (8) years or a fine of not more than Fifty Thousand Dollars ($50,000.00), or both.

              (D)  If three hundred (300) or more grams or one thousand (1,000) or more dosage units, but less than five hundred (500) grams or two thousand five hundred (2,500) dosage units, by imprisonment for not less than four (4) years nor more than sixteen (16) years or a fine of not more than Two Hundred Fifty Thousand Dollars ($250,000.00), or both.

     (d)  Paraphernalia.  (1)  Except as otherwise provided under subsection (i) of this section for actions that are lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder, it is unlawful for a person who is not authorized by the State Board of Medical Licensure, State Board of Pharmacy, or other lawful authority to use, or to possess with intent to use, paraphernalia to plant, propagate, cultivate, grow, harvest, manufacture, compound, convert, produce, process, prepare, test, analyze, pack, repack, store, contain, conceal, inject, ingest, inhale or otherwise introduce into the human body a controlled substance in violation of the Uniform Controlled Substances Law.  Any person who violates this subsection (d)(1) is guilty of a misdemeanor and, upon conviction, may be confined in the county jail for not more than six (6) months, or fined not more than Five Hundred Dollars ($500.00), or both; however, no person shall be charged with a violation of this subsection when such person is also charged with the possession of thirty (30) grams or less of marijuana under subsection (c)(2)(A) of this section.

          (2)  It is unlawful for any person to deliver, sell, possess with intent to deliver or sell, or manufacture with intent to deliver or sell, paraphernalia, knowing, or under circumstances where one reasonably should know, that it will be used to plant, propagate, cultivate, grow, harvest, manufacture, compound, convert, produce, process, prepare, test, analyze, pack, repack, store, contain, conceal, inject, ingest, inhale, or otherwise introduce into the human body a controlled substance in violation of the Uniform Controlled Substances Law.  Except as provided in subsection (d)(3), a person who violates this subsection (d)(2) is guilty of a misdemeanor and, upon conviction, may be confined in the county jail for not more than six (6) months, or fined not more than Five Hundred Dollars ($500.00), or both.

          (3)  Any person eighteen (18) years of age or over who violates subsection (d)(2) of this section by delivering or selling paraphernalia to a person under eighteen (18) years of age who is at least three (3) years his or her junior is guilty of a misdemeanor and, upon conviction, may be confined in the county jail for not more than one (1) year, or fined not more than One Thousand Dollars ($1,000.00), or both.

          (4)  It is unlawful for any person to place in any newspaper, magazine, handbill, or other publication any advertisement, knowing, or under circumstances where one reasonably should know, that the purpose of the advertisement, in whole or in part, is to promote the sale of objects designed or intended for use as paraphernalia.  Any person who violates this subsection is guilty of a misdemeanor and, upon conviction, may be confined in the county jail for not more than six (6) months, or fined not more than Five Hundred Dollars ($500.00), or both.

     (e)  It shall be unlawful for any physician practicing medicine in this state to prescribe, dispense or administer any amphetamine or amphetamine-like anorectics and/or central nervous system stimulants classified in Schedule II, pursuant to Section 41-29-115, for the exclusive treatment of obesity, weight control or weight loss.  Any person who violates this subsection, upon conviction, is guilty of a misdemeanor and may be confined for a period not to exceed six (6) months, or fined not more than One Thousand Dollars ($1,000.00), or both.

     (f)  Trafficking.  (1)  Any person trafficking in controlled substances shall be guilty of a felony and, upon conviction, shall be imprisoned for a term of not less than ten (10) years nor more than forty (40) years and shall be fined not less than Five Thousand Dollars ($5,000.00) nor more than One Million Dollars ($1,000,000.00).  The ten-year mandatory sentence shall not be reduced or suspended.  The person shall not be eligible for probation or parole, the provisions of Sections 41-29-149, 47-5-139, 47-7-3 and 47-7-33, to the contrary notwithstanding.

          (2)  "Trafficking in controlled substances" as used herein means:

              (A)  A violation of subsection (a) of this section involving thirty (30) or more grams or forty (40) or more dosage units of a Schedule I or II controlled substance except marijuana and synthetic cannabinoids;

              (B)  A violation of subsection (a) of this section involving five hundred (500) or more grams or two thousand five hundred (2,500) or more dosage units of a Schedule III, IV or V controlled substance;

              (C)  A violation of subsection (c) of this section involving thirty (30) or more grams or forty (40) or more dosage units of a Schedule I or II controlled substance except marijuana and synthetic cannabinoids;

              (D)  A violation of subsection (c) of this section involving five hundred (500) or more grams or two thousand five hundred (2,500) or more dosage units of a Schedule III, IV or V controlled substance; or

              (E)  A violation of subsection (a) of this section involving one (1) kilogram or more of marijuana or two hundred (200) grams or more of synthetic cannabinoids.

     (g)  Aggravated trafficking.  Any person trafficking in Schedule I or II controlled substances, except marijuana and synthetic cannabinoids, of two hundred (200) grams or more shall be guilty of aggravated trafficking and, upon conviction, shall be sentenced to a term of not less than twenty-five (25) years nor more than life in prison and shall be fined not less than Five Thousand Dollars ($5,000.00) nor more than One Million Dollars ($1,000,000.00).  The twenty-five-year sentence shall be a mandatory sentence and shall not be reduced or suspended.  The person shall not be eligible for probation or parole, the provisions of Sections 41-29-149, 47-5-139, 47-7-3 and 47-7-33, to the contrary notwithstanding.

     (h)  Sentence mitigation.  (1)  Notwithstanding any provision of this section, a person who has been convicted of an offense under this section that requires the judge to impose a prison sentence which cannot be suspended or reduced and is ineligible for probation or parole may, at the discretion of the court, receive a sentence of imprisonment that is no less than twenty-five percent (25%) of the sentence prescribed by the applicable statute.  In considering whether to apply the departure from the sentence prescribed, the court shall conclude that:

              (A)  The offender was not a leader of the criminal enterprise;

              (B)  The offender did not use violence or a weapon during the crime;

              (C)  The offense did not result in a death or serious bodily injury of a person not a party to the criminal enterprise; and

              (D)  The interests of justice are not served by the imposition of the prescribed mandatory sentence.

     The court may also consider whether information and assistance were furnished to a law enforcement agency, or its designee, which, in the opinion of the trial judge, objectively should or would have aided in the arrest or prosecution of others who violate this subsection.  The accused shall have adequate opportunity to develop and make a record of all information and assistance so furnished.

          (2)  If the court reduces the prescribed sentence pursuant to this subsection, it must specify on the record the circumstances warranting the departure.

     (i)  This section does not apply to any of the actions that are lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder.

     SECTION 28.  Section 41-29-141, Mississippi Code of 1972, is amended as follows:

     41-29-141.  It is unlawful for any person:

          (1)  Who is subject to Section 41-29-125 to distribute or dispense a controlled substance in violation of Section 41-29-137;

          (2)  Who is a registrant under Section 41-29-125 to manufacture a controlled substance not authorized by his or her registration, or to distribute or dispense a controlled substance not authorized by his or her registration to another registrant or other authorized person;

          (3)  To refuse or fail to make, keep or furnish any record, notification, order form, statement, invoice or information required under this article;

          (4)  To refuse a lawful entry into any premises for any inspection authorized by this article; or

          (5)  Knowingly to keep or maintain any store, shop, warehouse, dwelling, building, vehicle, boat, aircraft, or other structure or place, which is resorted to by persons using controlled substances in violation of this article for the purpose of using these substances, or which is used for keeping or selling them in violation of this article.

     Any person who violates this section shall, with respect to such violation, be subject to a civil penalty payable to the State of Mississippi of not more than Twenty-five Thousand Dollars ($25,000.00).

     In addition to the civil penalty provided in the preceding paragraph, any person who knowingly or intentionally violates this section shall be guilty of a crime and upon conviction thereof may be confined for a period of not more than one (1) year or fined not more than One Thousand Dollars ($1,000.00), or both.

     This section does not apply to any of the actions that are lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder.

     SECTION 29.  Section 41-29-143, Mississippi Code of 1972, is amended as follows:

     41-29-143.  It is unlawful for any person knowingly or intentionally:

          (1)  To distribute as a registrant a controlled substance classified in Schedule I or II, as set out in Sections 41-29-113 and 41-29-115, except pursuant to an order form as required by Section 41-29-135;

          (2)  To use in the course of the manufacture or distribution of a controlled substance a registration number which is fictitious, revoked, suspended, or issued to another person * * *.;

          (3)  To furnish false or fraudulent material information in, or omit any material information from, any application, report, or other document required to be kept or filed under this article, or any record required to be kept by this article; or

          (4)  To make, distribute, or possess any punch, die, plate, stone, or other thing designed to print, imprint, or reproduce the trademark, trade name, or other identifying mark, imprint or device of another or any likeness of any of the foregoing upon any drug or container or labeling thereof so as to render the drug a counterfeit substance.

     Any person who violates this section is guilty of a crime and upon conviction may be confined for not more than one (1) year or fined not more than One Thousand Dollars ($1,000.00) or both.

     This section does not apply to any of the actions that are lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder.

     SECTION 30.  Section 59-23-7, Mississippi Code of 1972, is amended as follows:

     59-23-7.  (1)  It is unlawful for any person to operate a watercraft on the public waters of this state who:

          (a)  Is under the influence of intoxicating liquor;

          (b)  Is under the influence of any other substance which has impaired such person's ability to operate a watercraft; or

          (c)  Has eight one-hundredths percent (.08%) or more by weight volume of alcohol in the person's blood based upon milligrams of alcohol per one hundred (100) cubic centimeters of blood as shown by a chemical analysis of such person's breath, blood or urine administered as authorized by this chapter.

     (2)  (a)  Except as provided in subsection (6) of this section, upon conviction of any person for the first offense of violating subsection (1) of this section where chemical tests provided for under Section 59-23-5 were given, or where chemical test results are not available, such person shall be fined not less than Two Hundred Fifty Dollars ($250.00) nor more than One Thousand Dollars ($1,000.00), or imprisoned for not more than twenty-four (24) hours in jail, or both; and the court shall order such person to attend and complete a boating safety education course developed by the Department of Wildlife, Fisheries and Parks.

          (b)  Upon any second conviction of any person violating subsection (1) of this section, the offenses being committed within a period of five (5) years, the person shall be fined not less than Six Hundred Dollars ($600.00) nor more than One Thousand Dollars ($1,000.00) and shall be imprisoned not less than forty-eight (48) consecutive hours nor more than one (1) year or sentenced to community service work for not less than ten (10) days nor more than one (1) year.  The court shall order the person not to operate a watercraft for one (1) year.

          (c)  For any third conviction of any person violating subsection (1) of this section, the offenses being committed within a period of five (5) years, the person shall be fined not less than Eight Hundred Dollars ($800.00) nor more than One Thousand Dollars ($1,000.00) and shall be imprisoned not less than thirty (30) days nor more than one (1) year.  The court shall order the person not to operate a watercraft for two (2) years.

          (d)  Any fourth or subsequent violation of subsection (1) of this section shall be a felony offense and, upon conviction, the offenses being committed within a period of five (5) years, the person shall be fined not less than Two Thousand Dollars ($2,000.00) nor more than Five Thousand Dollars ($5,000.00) and shall be imprisoned not less than ninety (90) days nor more than five (5) years in the custody of the Department of Corrections.  The court shall order the person not to operate a watercraft for three (3) years.

     (3)  Any person convicted of operating any watercraft in violation of subsection (1) of this section where the person (a) refused a law enforcement officer's request to submit to a chemical test, or (b) was unconscious at the time of a chemical test and refused to consent to the introduction of the results of such test in any prosecution, shall be punished consistent with the penalties prescribed herein for persons submitting to the test and the court shall order the person not to operate a watercraft for the time periods specified in subsection (2) of this section.

     (4)  Any person who operates any watercraft in violation of the provisions of subsection (1) of this section and who in a negligent manner causes the death of another or mutilates, disfigures, permanently disables or destroys the tongue, eye, lip, nose or any other member or limb of another shall, upon conviction, be guilty of a felony and shall be committed to the custody of the Department of Corrections for a period of time not to exceed ten (10) years.

     (5)  Upon conviction of any violation of subsection (1) of this section, the judge shall cause a copy of the citation and any other pertinent documents concerning the conviction to be sent immediately to the Mississippi Department of Wildlife, Fisheries and Parks and the Department of Marine Resources.  A copy of the citation or other pertinent documents, having been attested as true and correct by the Director of the Mississippi Department of Wildlife, Fisheries and Parks, or his or her designee, or the Director of the Department of Marine Resources, or his or her designee, shall be sufficient proof of the conviction for purposes of determining the enhanced penalty for any subsequent convictions of violations of subsection (1) of this section.

     (6)  A registered qualified patient of medical cannabis under the Mississippi Medical Cannabis Compassion Act who operates a watercraft within this state while under the influence of medical cannabis shall be subject to the penalties set forth in Section 10(7) of this act for his or her first offense and shall not be subject to the penalties under subsection (2)(a) of this section.  All other provisions of this section are applicable to first offenses under Section 10(7) of this act and all second and subsequent offenses by registered qualified patients.

     SECTION 31.  Section 63-11-30, Mississippi Code of 1972, is amended as follows:

     63-11-30.  (1)  It is unlawful for a person to drive or otherwise operate a vehicle within this state if the person:

          (a)  Is under the influence of intoxicating liquor;

          (b)  Is under the influence of any other substance that has impaired the person's ability to operate a motor vehicle;

          (c)  Is under the influence of any drug or controlled substance, the possession of which is unlawful under the Mississippi Controlled Substances Law; or

          (d)  Has an alcohol concentration in the person's blood, based upon grams of alcohol per one hundred (100) milliliters of blood, or grams of alcohol per two hundred ten (210) liters of breath, as shown by a chemical analysis of the person's breath, blood or urine administered as authorized by this chapter, of:

              (i)  Eight one-hundredths percent (.08%) or more for a person who is above the legal age to purchase alcoholic beverages under state law;

               (ii)  Two one-hundredths percent (.02%) or more for a person who is below the legal age to purchase alcoholic beverages under state law; or

              (iii)  Four one-hundredths percent (.04%) or more for a person operating a commercial motor vehicle.

     (2)  Except as otherwise provided in subsection (3) of this section (Zero Tolerance for Minors):

          (a)  First offense DUI.  (i)  Except as provided in subsection (15) of this section, upon conviction of any person for the first offense of violating subsection (1) of this section where chemical tests under Section 63-11-5 were given, or where chemical test results are not available, the person shall be fined not less than Two Hundred Fifty Dollars ($250.00) nor more than One Thousand Dollars ($1,000.00), or imprisoned for not more than forty-eight (48) hours in jail, or both; the court shall order the person to attend and complete an alcohol safety education program as provided in Section 63-11-32 within six (6) months of sentencing.  The court may substitute attendance at a victim impact panel instead of forty-eight (48) hours in jail.

              (ii)  Suspension of commercial driving privileges is governed by Section 63-1-216.

              (iii)  A qualifying first offense may be nonadjudicated by the court under subsection (14) of this section.  The holder of a commercial driver's license or a commercial learning permit at the time of the offense is ineligible for nonadjudication.

              (iv)  Eligibility for an interlock-restricted license is governed by Section 63-11-31 and suspension of regular driving privileges is governed by Section 63-11-23.

          (b)  Second offense DUI.  (i)  Upon any second conviction of any person violating subsection (1) of this section, the offenses being committed within a period of five (5) years, the person shall be guilty of a misdemeanor, fined not less than Six Hundred Dollars ($600.00) nor more than One Thousand Five Hundred Dollars ($1,500.00), shall be imprisoned not less than five (5) days nor more than six (6) months and sentenced to community service work for not less than ten (10) days nor more than six (6) months.  The minimum penalties shall not be suspended or reduced by the court and no prosecutor shall offer any suspension or sentence reduction as part of a plea bargain.

              (ii)  Suspension of commercial driving privileges is governed by Section 63-1-216.

              (iii)  Eligibility for an interlock-restricted license is governed by Section 63-11-31 and suspension of regular driving privileges is governed by Section 63-11-23.

          (c)  Third offense DUI.  (i)  For a third conviction of a person for violating subsection (1) of this section, the offenses being committed within a period of five (5) years, the person shall be guilty of a felony and fined not less than Two Thousand Dollars ($2,000.00) nor more than Five Thousand Dollars ($5,000.00), and shall serve not less than one (1) year nor more than five (5) years in the custody of the Department of Corrections.  For any offense that does not result in serious injury or death to any person, the sentence of incarceration may be served in the county jail rather than in the State Penitentiary at the discretion of the circuit court judge.  The minimum penalties shall not be suspended or reduced by the court and no prosecutor shall offer any suspension or sentence reduction as part of a plea bargain.

              (ii)  The suspension of commercial driving privileges is governed by Section 63-1-216.

              (iii)  The suspension of regular driving privileges is governed by Section 63-11-23.

          (d)  Fourth and subsequent offense DUI.  (i)  For any fourth or subsequent conviction of a violation of subsection (1) of this section, without regard to the time period within which the violations occurred, the person shall be guilty of a felony and fined not less than Three Thousand Dollars ($3,000.00) nor more than Ten Thousand Dollars ($10,000.00), and shall serve not less than two (2) years nor more than ten (10) years in the custody of the Department of Corrections.

              (ii)  The suspension of commercial driving privileges is governed by Section 63-1-216.

               (iii)  A person convicted of a fourth or subsequent offense is ineligible to exercise the privilege to operate a motor vehicle that is not equipped with an ignition-interlock device for ten (10) years.

          (e)  Any person convicted of a second or subsequent violation of subsection (1) of this section shall receive an in-depth diagnostic assessment, and if as a result of the assessment is determined to be in need of treatment for alcohol or drug abuse, the person must successfully complete treatment at a program site certified by the Department of Mental Health.  Each person who receives a diagnostic assessment shall pay a fee representing the cost of the assessment.  Each person who participates in a treatment program shall pay a fee representing the cost of treatment.

          (f)  The use of ignition-interlock devices is governed by Section 63-11-31.

     (3)  Zero Tolerance for Minors.  (a)  This subsection shall be known and may be cited as Zero Tolerance for Minors.  The provisions of this subsection shall apply only when a person under the age of twenty-one (21) years has a blood alcohol concentration of two one-hundredths percent (.02%) or more, but lower than eight one-hundredths percent (.08%).  If the person's blood alcohol concentration is eight one-hundredths percent (.08%) or more, the provisions of subsection (2) shall apply.

          (b)  (i)  A person under the age of twenty-one (21) is eligible for nonadjudication of a qualifying first offense by the court pursuant to subsection (14) of this section.

              (ii)  Upon conviction of any person under the age of twenty-one (21) years for the first offense of violating subsection (1) of this section where chemical tests provided for under Section 63-11-5 were given, or where chemical test results are not available, the person shall be fined Two Hundred Fifty Dollars ($250.00); the court shall order the person to attend and complete an alcohol safety education program as provided in Section 63-11-32 within six (6) months.  The court may also require attendance at a victim impact panel.

          (c)  A person under the age of twenty-one (21) years who is convicted of a second violation of subsection (1) of this section, the offenses being committed within a period of five (5) years, shall be fined not more than Five Hundred Dollars ($500.00).

          (d)  A person under the age of twenty-one (21) years who is convicted of a third or subsequent violation of subsection (1) of this section, the offenses being committed within a period of five (5) years, shall be fined not more than One Thousand Dollars ($1,000.00).

          (e)  License suspension is governed by Section 63-11-23 and ignition interlock is governed by Section 63-11-31.

          (f)  Any person under the age of twenty-one (21) years convicted of a third or subsequent violation of subsection (1) of this section must complete treatment of an alcohol or drug abuse program at a site certified by the Department of Mental Health.

     (4)  DUI test refusal.  In addition to the other penalties provided in this section, every person refusing a law enforcement officer's request to submit to a chemical test of the person's breath as provided in this chapter, or who was unconscious at the time of a chemical test and refused to consent to the introduction of the results of the test in any prosecution, shall suffer an additional administrative suspension of driving privileges as set forth in Section 63-11-23.

     (5)  Aggravated DUI.  (a)  Every person who operates any motor vehicle in violation of the provisions of subsection (1) of this section and who in a negligent manner causes the death of another or mutilates, disfigures, permanently disables or destroys the tongue, eye, lip, nose or any other limb, organ or member of another shall, upon conviction, be guilty of a separate felony for each victim who suffers death, mutilation, disfigurement or other injury and shall be committed to the custody of the State Department of Corrections for a period of time of not less than five (5) years and not to exceed twenty-five (25) years for each death, mutilation, disfigurement or other injury, and the imprisonment for the second or each subsequent conviction, in the discretion of the court, shall commence either at the termination of the imprisonment for the preceding conviction or run concurrently with the preceding conviction.  Any person charged with causing the death of another as described in this subsection shall be required to post bail before being released after arrest.

          (b)  A holder of a commercial driver's license who is convicted of operating a commercial motor vehicle with an alcohol concentration of eight one- * * *hundrethshundredths percent (.08%) or more shall be guilty of a felony and shall be committed to the custody of the Department of Corrections for not less than two (2) years and not more than ten (10) years.

          (c)  The court shall order an ignition-interlock restriction on the offender's privilege to drive as a condition of probation or post-release supervision not to exceed five (5) years unless a longer restriction is required under other law.  The ignition-interlock restriction shall not be applied to commercial license privileges until the driver serves the full disqualification period required by Section 63-1-216.

     (6)  DUI citations.  (a)  Upon conviction of a violation of subsection (1) of this section, the trial judge shall sign in the place provided on the traffic ticket, citation or affidavit stating that the person arrested either employed an attorney or waived his or her right to an attorney after having been properly advised.  If the person arrested employed an attorney, the name, address and telephone number of the attorney shall be written on the ticket, citation or affidavit.  The court clerk must immediately send a copy of the traffic ticket, citation or affidavit, and any other pertinent documents concerning the conviction or other order of the court, to the Department of Public Safety as provided in Section 63-11-37.

          (b)  A copy of the traffic ticket, citation or affidavit and any other pertinent documents, having been attested as true and correct by the Commissioner of Public Safety, or his or her designee, shall be sufficient proof of the conviction for purposes of determining the enhanced penalty for any subsequent convictions of violations of subsection (1) of this section.  The Department of Public Safety shall maintain a central database for verification of prior offenses and convictions.

     (7)  Out-of-state prior convictions.  Convictions in another state, territory or possession of the United States, or under the law of a federally recognized Native American tribe, of violations for driving or operating a vehicle while under the influence of an intoxicating liquor or while under the influence of any other substance that has impaired the person's ability to operate a motor vehicle occurring within five (5) years before an offense shall be counted for the purposes of determining if a violation of subsection (1) of this section is a second, third, fourth or subsequent offense and the penalty that shall be imposed upon conviction for a violation of subsection (1) of this section.

     (8)  Charging of subsequent offenses.  (a)  For the purposes of determining how to impose the sentence for a second, third, fourth or subsequent conviction under this section, the affidavit or indictment shall not be required to enumerate previous convictions.  It shall only be necessary that the affidavit or indictment states the number of times that the defendant has been convicted and sentenced within the past five (5) years for a second or third offense, or without a time limitation for a fourth or subsequent offense, under this section to determine if an enhanced penalty shall be imposed.  The amount of fine and imprisonment imposed in previous convictions shall not be considered in calculating offenses to determine a second, third, fourth or subsequent offense of this section.

          (b)  Before a defendant enters a plea of guilty to an offense under this section, law enforcement must submit certification to the prosecutor that the defendant's driving record, the confidential registry and National Crime Information Center record have been searched for all prior convictions, nonadjudications, pretrial diversions and arrests for driving or operating a vehicle while under the influence of an intoxicating liquor or while under the influence of any other substance that has impaired the person's ability to operate a motor vehicle.  The results of the search must be included in the certification.

     (9)  License eligibility for underage offenders.  A person who is under the legal age to obtain a license to operate a motor vehicle at the time of the offense and who is convicted under this section shall not be eligible to receive a driver's license until the person reaches the age of eighteen (18) years.

     (10)  License suspensions and restrictions to run consecutively.  Suspension or restriction of driving privileges for any person convicted of or nonadjudicated for violations of subsection (1) of this section shall run consecutively to and not concurrently with any other administrative license suspension.

     (11)  Ignition interlock.  If the court orders installation and use of an ignition-interlock device as provided in Section 63-11-31 for every vehicle operated by a person convicted or nonadjudicated under this section, each device shall be installed, maintained and removed as provided in Section 63-11-31.

     (12)  DUI child endangerment.  A person over the age of twenty-one (21) who violates subsection (1) of this section while transporting in a motor vehicle a child under the age of sixteen (16) years is guilty of the separate offense of endangering a child by driving under the influence of alcohol or any other substance which has impaired the person's ability to operate a motor vehicle.  The offense of endangering a child by driving under the influence of alcohol or any other substance which has impaired the person's ability to operate a motor vehicle shall not be merged with an offense of violating subsection (1) of this section for the purposes of prosecution and sentencing.  An offender who is convicted of a violation of this subsection shall be punished as follows:

          (a)  A person who commits a violation of this subsection which does not result in the serious injury or death of a child and which is a first conviction shall be guilty of a misdemeanor and, upon conviction, shall be fined not more than One Thousand Dollars ($1,000.00) or shall be imprisoned for not more than twelve (12) months, or both;

          (b)  A person who commits a violation of this subsection which does not result in the serious injury or death of a child and which is a second conviction shall be guilty of a misdemeanor and, upon conviction, shall be fined not less than One Thousand Dollars ($1,000.00) nor more than Five Thousand Dollars ($5,000.00) or shall be imprisoned for one (1) year, or both;

          (c)  A person who commits a violation of this subsection which does not result in the serious injury or death of a child and which is a third or subsequent conviction shall be guilty of a felony and, upon conviction, shall be fined not less than Ten Thousand Dollars ($10,000.00) or shall be imprisoned for not less than one (1) year nor more than five (5) years, or both; and

          (d)  A person who commits a violation of this subsection which results in the serious injury or death of a child, without regard to whether the offense was a first, second, third or subsequent offense, shall be guilty of a felony and, upon conviction, shall be punished by a fine of not less than Ten Thousand Dollars ($10,000.00) and shall be imprisoned for not less than five (5) years nor more than twenty-five (25) years.

     (13)  Expunction.  (a)  Any person convicted under subsection (2) or (3) of this section of a first offense of driving under the influence and who was not the holder of a commercial driver's license or a commercial learning permit at the time of the offense may petition the circuit court of the county in which the conviction was had for an order to expunge the record of the conviction at least five (5) years after successful completion of all terms and conditions of the sentence imposed for the conviction.  Expunction under this subsection will only be available to a person:

              (i)  Who has successfully completed all terms and conditions of the sentence imposed for the conviction;

              (ii)  Who did not refuse to submit to a test of his or her blood or breath;

              (iii)  Whose blood alcohol concentration tested below sixteen one-hundredths percent (.16%) if test results are available;

              (iv)  Who has not been convicted of and does not have pending any other offense of driving under the influence;

              (v)  Who has provided the court with justification as to why the conviction should be expunged; and

              (vi)  Who has not previously had a nonadjudication or expunction of a violation of this section.

          (b)  A person is eligible for only one (1) expunction under this subsection, and the Department of Public Safety shall maintain a permanent confidential registry of all cases of expunction under this subsection for the sole purpose of determining a person's eligibility for expunction, for nonadjudication, or as a first offender under this section.

          (c)  The court in its order of expunction shall state in writing the justification for which the expunction was granted and forward the order to the Department of Public Safety within five (5) days of the entry of the order.

     (14)  Nonadjudication.  (a)  For the purposes of this chapter, "nonadjudication" means that the court withholds adjudication of guilt and sentencing, either at the conclusion of a trial on the merits or upon the entry of a plea of guilt by a defendant, and places the defendant in a nonadjudication program conditioned upon the successful completion of the requirements imposed by the court under this subsection.

          (b)  A person is eligible for nonadjudication of an offense under this Section 63-11-30 only one (1) time under any provision of a law that authorizes nonadjudication and only for an offender:

               (i)  Who has successfully completed all terms and conditions imposed by the court after placement of the defendant in a nonadjudication program;

               (ii)  Who was not the holder of a commercial driver's license or a commercial learning permit at the time of the offense;

               (iii)  Who has not previously been convicted of and does not have pending any former or subsequent charges under this section; and

              (iv)  Who has provided the court with justification as to why nonadjudication is appropriate.

          (c)  Nonadjudication may be initiated upon the filing of a petition for nonadjudication or at any stage of the proceedings in the discretion of the court; the court may withhold adjudication of guilt, defer sentencing, and upon the agreement of the offender to participate in a nonadjudication program, enter an order imposing requirements on the offender for a period of court supervision before the order of nonadjudication is entered.  Failure to successfully complete a nonadjudication program subjects the person to adjudication of the charges against him or her and to imposition of all penalties previously withheld due to entrance into a nonadjudication program.  The court shall immediately inform the commissioner of the conviction as required in Section 63-11-37.

              (i)  The court shall order the person to:

                   1.  Pay the nonadjudication fee imposed under Section 63-11-31 if applicable;

                   2.  Pay all fines, penalties and assessments that would have been imposed for conviction;

                    3.  Attend and complete an alcohol safety education program as provided in Section 63-11-32 within six (6) months of the date of the order;

                   4.  a.  If the court determines that the person violated this section with respect to alcohol or intoxicating liquor, the person must install an ignition-interlock device on every motor vehicle operated by the person, obtain an interlock-restricted license, and maintain that license for one hundred twenty (120) days or suffer a one-hundred-twenty-day suspension of the person's regular driver's license, during which time the person must not operate any vehicle.

                        b.  If the court determines that the person violated this section by operating a vehicle when under the influence of a substance other than alcohol that has impaired the person's ability to operate a motor vehicle, including any drug or controlled substance which is unlawful to possess under the Mississippi Controlled Substances Law, the person must submit to a one-hundred-twenty-day period of a nonadjudication program that includes court-ordered drug testing at the person's own expense not less often than every thirty (30) days, during which time the person may drive if compliant with the terms of the program, or suffer a one-hundred-twenty-day suspension of the person's regular driver's license, during which time the person will not operate any vehicle.

              (ii)  Other conditions that may be imposed by the court include, but are not limited to, alcohol or drug screening, or both, proof that the person has not committed any other traffic violations while under court supervision, proof of immobilization or impoundment of vehicles owned by the offender if required, and attendance at a victim-impact panel.

          (d)  The court may enter an order of nonadjudication only if the court finds, after a hearing or after ex parte examination of reliable documentation of compliance, that the offender has successfully completed all conditions imposed by law and previous orders of the court.  The court shall retain jurisdiction over cases involving nonadjudication for a period of not more than two (2) years.

          (e)  (i)  The clerk shall immediately forward a record of every person placed in a nonadjudication program and of every nonadjudication order to the Department of Public Safety for inclusion in the permanent confidential registry of all cases that are nonadjudicated under this subsection (14).

              (ii)  Judges, clerks and prosecutors involved in the trial of implied consent violations and law enforcement officers involved in the issuance of citations for implied consent violations shall have secure online access to the confidential registry for the purpose of determining whether a person has previously been the subject of a nonadjudicated case and 1. is therefore ineligible for another nonadjudication; 2. is ineligible as a first offender for a violation of this section; or 3. is ineligible for expunction of a conviction of a violation of this section.

              (iii)  The Driver Services Bureau of the department shall have access to the confidential registry for the purpose of determining whether a person is eligible for a form of license not restricted to operating a vehicle equipped with an ignition-interlock device.

              (iv)  The Mississippi Alcohol Safety Education Program shall have secure online access to the confidential registry for research purposes only.

     (15)  A registered qualified patient of medical cannabis under the Mississippi Medical Cannabis Compassion Act who drives or otherwise operates a motor vehicle within this state while under the influence of medical cannabis shall be subject to the penalties set forth in Section 10(7) of this act for his or her first offense and shall not be subject to the penalties under subsection 2(a) of this section.  All other provisions of this section are applicable to first offenses under Section 10(7) of this act and all second and subsequent offenses by registered qualified patients.

     SECTION 32.  Section 71-3-7, Mississippi Code of 1972, is amended as follows:

     71-3-7.  (1)  Compensation shall be payable for disability or death of an employee from injury or occupational disease arising out of and in the course of employment, without regard to fault as to the cause of the injury or occupational disease.  An occupational disease shall be deemed to arise out of and in the course of employment when there is evidence that there is a direct causal connection between the work performed and the occupational disease.  In all claims in which no benefits, including disability, death and medical benefits, have been paid, the claimant shall file medical records in support of his or her claim for benefits when filing a petition to controvert.  If the claimant is unable to file the medical records in support of his or her claim for benefits at the time of filing the petition to controvert because of a limitation of time established by Section 71-3-35 or Section 71-3-53, the claimant shall file medical records in support of his or her claim within sixty (60) days after filing the petition to controvert.

     (2)  Where a preexisting physical handicap, disease, or lesion is shown by medical findings to be a material contributing factor in the results following injury, the compensation which, but for this subsection, would be payable shall be reduced by that proportion which such preexisting physical handicap, disease, or lesion contributed to the production of the results following the injury.  The preexisting condition does not have to be occupationally disabling for this apportionment to apply.

     (3)  The following provisions shall apply to subsections (1) and (2) of this section:

          (a)  Apportionment shall not be applied until the claimant has reached maximum medical recovery.

          (b)  The employer or carrier does not have the power to determine the date of maximum medical recovery or percentage of apportionment.  This must be done by the attorney-referee, subject to review by the commission as the ultimate finder of fact.

          (c)  After the date the claimant reaches maximum medical recovery, weekly compensation benefits and maximum recovery shall be reduced by that proportion which the preexisting physical handicap, disease, or lesion contributes to the results following injury.

          (d)  If maximum medical recovery has occurred before the hearing and order of the attorney-referee, credit for excess payments shall be allowed in future payments.  Such allowances and method of accomplishment of the same shall be determined by the attorney-referee, subject to review by the commission.  However, no actual repayment of such excess shall be made to the employer or carrier.

     (4)  No compensation shall be payable if the use of drugs illegally, or the use of a valid prescription medication(s) taken contrary to the prescriber's instructions and/or contrary to label warnings, or the use of medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act and rules and regulations adopted thereunder, or intoxication due to the use of alcohol of the employee was the proximate cause of the injury, or if it was the willful intention of the employee to injure or kill himself or herself or another.

     (5)  Every employer to whom this chapter applies shall be liable for and shall secure the payment to his or her employees of the compensation payable under its provisions.

     (6)  In the case of an employer who is a subcontractor, the contractor shall be liable for and shall secure the payment of such compensation to employees of the subcontractor, unless the subcontractor has secured such payment.

     SECTION 33.  Section 71-3-121, Mississippi Code of 1972, is amended as follows:

     71-3-121.  (1)  In the event that an employee sustains an injury at work or asserts a work-related injury, the employer shall have the right to administer drug and alcohol testing or require that the employee submit himself or herself to drug and alcohol testing.  If the employee has a positive test indicating the presence, at the time of injury, of any drug illegally used or the use of a valid prescription medication(s) taken contrary to the prescriber's instructions and/or contrary to label warnings, or the use of medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act and rules and regulations adopted thereunder, or eight one-hundredths percent (.08%) or more by weight volume of alcohol in the person's blood, it shall be presumed that the proximate cause of the injury was the use of a drug illegally, or the use of a valid prescription medication(s) taken contrary to the prescriber's instructions and/or contrary to label warnings, or the use of medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act and rules and regulations adopted thereunder, or the intoxication due to the use of alcohol by the employee.  If the employee refuses to submit himself or herself to drug and alcohol testing immediately after the alleged work-related injury, then it shall be presumed that the employee was using a drug illegally, or was using a valid prescription medication(s) contrary to the prescriber's instructions and/or contrary to label warnings, or the use of medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act and rules and regulations adopted thereunder, or was intoxicated due to the use of alcohol at the time of the accident and that the proximate cause of the injury was the use of a drug illegally, or the use of a valid prescription medication(s) taken contrary to the prescriber's instructions and/or contrary to label warnings, or the use of medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act and rules and regulations adopted thereunder, or the intoxication due to the use of alcohol of the employee.  The burden of proof will then be placed upon the employee to prove that the use of drugs illegally, or the use of a valid prescription medication(s) taken contrary to the prescriber's instructions and/or contrary to label warnings, or the use of medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act and rules and regulations adopted thereunder, or intoxication due to the use of alcohol was not a contributing cause of the accident in order to defeat the defense of the employer provided under Section 71-3-7.

     (2)  The results of the drug and alcohol tests, employer-administered or otherwise, shall be considered admissible evidence solely on the issue of causation in the determination of the use of drugs illegally, or the use of a valid prescription medication(s) taken contrary to the prescriber's instructions and/or contrary to label warnings, or the use of medical cannabis in accordance with the Mississippi Medical Cannabis Compassion Act and rules and regulations adopted thereunder, or the intoxication due to the use of alcohol of an employee at the time of injury for workers' compensation purposes under Section 71-3-7.

     (3)  No cause of action for defamation of character, libel, slander or damage to reputation arises in favor of any person against an employer under the provisions of this section.

     SECTION 34.  Section 73-21-73, Mississippi Code of 1972, is amended as follows:

     73-21-73.  As used in this chapter, unless the context requires otherwise:

          (a)  "Administer" means the direct application of a prescription drug pursuant to a lawful order of a practitioner to the body of a patient by injection, inhalation, ingestion or any other means.

          (b)  "Biological product" means the same as that term is defined in 42 USC Section 262.

          (c)  "Board of Pharmacy," "Pharmacy Board," "MSBP" or "board" means the State Board of Pharmacy.

          (d)  "Compounding" means (i) the production, preparation, propagation, conversion or processing of a sterile or nonsterile drug or device either directly or indirectly by extraction from substances of natural origin or independently by means of chemical or biological synthesis or from bulk chemicals or the preparation, mixing, measuring, assembling, packaging or labeling of a drug or device as a result of a practitioner's prescription drug order or initiative based on the practitioner/patient/pharmacist relationship in the course of professional practice, or (ii) for the purpose of, as an incident to, research, teaching or chemical analysis and not for sale or dispensing.  Compounding also includes the preparation of drugs or devices in anticipation of prescription drug orders based on routine regularly observed prescribing patterns.

          (e)  "Continuing education unit" means ten (10) clock hours of study or other such activity as may be approved by the board, including, but not limited to, all programs which have been approved by the American Council on Pharmaceutical Education.

          (f)  "Deliver" or "delivery" means the actual, constructive or attempted transfer in any manner of a drug or device from one (1) person to another, whether or not for a consideration, including, but not limited to, delivery by mailing or shipping.

          (g)  "Device" means an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent or other similar or related article, including any component part or accessory which is required under federal or state law to be prescribed by a practitioner and dispensed by a pharmacist.

          (h)  "Dispense" or "dispensing" means the interpretation of a valid prescription of a practitioner by a pharmacist and the subsequent preparation of the drug or device for administration to or use by a patient or other individual entitled to receive the drug.

          (i)  "Distribute" means the delivery of a drug or device other than by administering or dispensing to persons other than the ultimate consumer.

          (j)  "Drug" means:

              (i)  Articles recognized as drugs in the official United States Pharmacopeia, official National Formulary, official Homeopathic Pharmacopeia, other drug compendium or any supplement to any of them;

              (ii)  Articles intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease in man or other animals;

              (iii)  Articles other than food intended to affect the structure or any function of the body of man or other animals; and

              (iv)  Articles intended for use as a component of any articles specified in subparagraph (i), (ii) or (iii) of this paragraph.

          (k)  "Drugroom" means a business, which does not require the services of a pharmacist, where prescription drugs or prescription devices are bought, sold, maintained or provided to consumers.

          (l)  "Extern" means a student in the professional program of a school of pharmacy accredited by the American Council on Pharmaceutical Education who is making normal progress toward completion of a professional degree in pharmacy.

          (m)  "Foreign pharmacy graduate" means a person whose undergraduate pharmacy degree was conferred by a recognized school of pharmacy outside of the United States, the District of Columbia and Puerto Rico.  Recognized schools of pharmacy are those colleges and universities listed in the World Health Organization's World Directory of Schools of Pharmacy, or otherwise approved by the Foreign Pharmacy Graduate Examination Committee (FPGEC) certification program as established by the National Association of Boards of Pharmacy.

          (n)  "Generic equivalent drug product" means a drug product which (i) contains the identical active chemical ingredient of the same strength, quantity and dosage form; (ii) is of the same generic drug name as determined by the United States Adoptive Names and accepted by the United States Food and Drug Administration; and (iii) conforms to such rules and regulations as may be adopted by the board for the protection of the public to assure that such drug product is therapeutically equivalent.

          (o)  "Interchangeable biological product" or "I.B." means a biological product that the federal Food and Drug Administration:

              (i)  Has licensed and determined as meeting the standards for interchangeability under 42 USC Section 262(k)(4); or

              (ii)  Has determined is therapeutically equivalent as set forth in the latest edition of or supplement to the federal Food and Drug Administration's Approved Drug Products with Therapeutic Equivalence Evaluations.

          (p)  "Internet" means collectively the myriad of computer and telecommunications facilities, including equipment and operating software, which comprise the interconnected worldwide network of networks that employ the Transmission Control Protocol/Internet Protocol, or any predecessor or successor protocol to such protocol, to communicate information of all kinds by wire or radio.

          (q)  "Interested directly" means being employed by, having full or partial ownership of, or control of, any facility permitted or licensed by the Mississippi State Board of Pharmacy.

          (r)  "Interested indirectly" means having a spouse who is employed by any facility permitted or licensed by the Mississippi State Board of Pharmacy.

          (s)  "Intern" means a person who has graduated from a school of pharmacy but has not yet become licensed as a pharmacist.

          (t)  "Manufacturer" means a person, business or other entity engaged in the production, preparation, propagation, conversion or processing of a prescription drug or device, if such actions are associated with promotion and marketing of such drugs or devices.

          (u)  "Manufacturer's distributor" means any person or business who is not an employee of a manufacturer, but who distributes sample drugs or devices, as defined under subsection (i) of this section, under contract or business arrangement for a manufacturer to practitioners.

          (v)  "Manufacturing" of prescription products means the production, preparation, propagation, conversion or processing of a drug or device, either directly or indirectly, by extraction from substances from natural origin or independently by means of chemical or biological synthesis, or from bulk chemicals and includes any packaging or repackaging of the substance(s) or labeling or relabeling of its container, if such actions are associated with promotion and marketing of such drug or devices.

          (w)  "Misappropriation of a prescription drug" means to illegally or unlawfully convert a drug, as defined in subsection (i) of this section, to one's own use or to the use of another.

          (x)  "Nonprescription drugs" means nonnarcotic medicines or drugs that may be sold without a prescription and are prepackaged and labeled for use by the consumer in accordance with the requirements of the statutes and regulations of this state and the federal government.

          (y)  "Person" means an individual, corporation, partnership, association or any other legal entity.

          (z)  "Pharmacist" means an individual health care provider licensed by this state to engage in the practice of pharmacy.  This recognizes a pharmacist as a learned professional who is authorized to provide patient services.

          (aa)  "Pharmacy" means any location for which a pharmacy permit is required and in which prescription drugs are maintained, compounded and dispensed for patients by a pharmacist.  This definition includes any location where pharmacy-related services are provided by a pharmacist.

          (bb)  "Prepackaging" means the act of placing small precounted quantities of drug products in containers suitable for dispensing or administering in anticipation of prescriptions or orders.

          (cc)  "Unlawful or unauthorized possession" means physical holding or control by a pharmacist of a controlled substance outside the usual and lawful course of employment.

          (dd)  "Practice of pharmacy" means a health care service that includes, but is not limited to, the compounding, dispensing, and labeling of drugs or devices; interpreting and evaluating prescriptions; administering and distributing drugs and devices; the compounding, dispensing and labeling of drugs and devices; maintaining prescription drug records; advising and consulting concerning therapeutic values, content, hazards and uses of drugs and devices; initiating or modifying of drug therapy in accordance with written guidelines or protocols previously established and approved by the board; selecting drugs; participating in drug utilization reviews; storing prescription drugs and devices; ordering lab work in accordance with written guidelines or protocols as defined by paragraph (nn) of this section; providing pharmacotherapeutic consultations; supervising supportive personnel and such other acts, services, operations or transactions necessary or incidental to the conduct of the foregoing.

          (ee)  "Practitioner" means a physician, dentist, veterinarian, or other health care provider authorized by law to diagnose and prescribe drugs.

          (ff)  "Prescription" means a written, verbal or electronically transmitted order issued by a practitioner for a drug or device to be dispensed for a patient by a pharmacist.  "Prescription" includes a standing order issued by a practitioner to an individual pharmacy that authorizes the pharmacy to dispense an opioid antagonist to certain persons without the person to whom the opioid antagonist is dispensed needing to have an individual prescription, as authorized by Section 41-29-319(3).  The term "prescription" does not include the recommendation of medical cannabis by a practitioner to a patient under the Mississippi Medical Cannabis Compassion Act.

          (gg)  "Prescription drug" or "legend drug" means a drug which is required under federal law to be labeled with either of the following statements prior to being dispensed or delivered:

              (i)  "Caution:  Federal law prohibits dispensing without prescription," or

              (ii)  "Caution:  Federal law restricts this drug to use by or on the order of a licensed veterinarian"; or a drug which is required by any applicable federal or state law or regulation to be dispensed on prescription only or is restricted to use by practitioners only.

          (hh)  "Product selection" means the dispensing of a generic equivalent drug product or an interchangeable biological product in lieu of the drug product ordered by the prescriber.

          (ii)  "Provider" or "primary health care provider" includes a pharmacist who provides health care services within his or her scope of practice pursuant to state law and regulation.

          (jj)  "Registrant" means a pharmacy or other entity which is registered with the Mississippi State Board of Pharmacy to buy, sell or maintain controlled substances.

          (kk)  "Repackager" means a person registered by the federal Food and Drug Administration as a repackager who removes a prescription drug product from its marketed container and places it into another, usually of smaller size, to be distributed to persons other than the consumer.

          (ll)  "Reverse distributor" means a business operator that is responsible for the receipt and appropriate return or disposal of unwanted, unneeded or outdated stocks of controlled or uncontrolled drugs from a pharmacy.

          (mm)  "Supportive personnel" or "pharmacist technician" means those individuals utilized in pharmacies whose responsibilities are to provide nonjudgmental technical services concerned with the preparation and distribution of drugs under the direct supervision and responsibility of a pharmacist.

          (nn)  "Written guideline or protocol" means an agreement in which any practitioner authorized to prescribe drugs delegates to a pharmacist authority to conduct specific prescribing functions in an institutional setting, or with the practitioner's individual patients, provided that a specific protocol agreement between the practitioner and the pharmacist is signed and filed as required by law or by rule or regulation of the board.

          (oo)  "Wholesaler" means a person who buys or otherwise acquires prescription drugs or prescription devices for resale or distribution, or for repackaging for resale or distribution, to persons other than consumers.

          (pp)  "Pharmacy benefit manager" has the same meaning as defined in Section 73-21-153.

     SECTION 35.  Section 73-21-127, Mississippi Code of 1972, is amended as follows:

     73-21-127.  (1)  The Board of Pharmacy shall develop and implement a computerized program to track prescriptions for controlled substances and to report suspected abuse and misuse of controlled substances in compliance with the federal regulations promulgated under authority of the National All Schedules Prescription Electronic Reporting Act of 2005 and in compliance with the federal HIPAA law, under the following conditions:

          (a)  Submission or reporting of dispensing information shall be mandatory and required by the State Board of Pharmacy for any entity dispensing controlled substances in or into the State of Mississippi, except for the dispensing of controlled substance drugs by a veterinarian residing in the State of Mississippi.

          (b)  The prescriptions tracked shall be prescriptions for controlled substances listed in Schedule II, III, IV or V and specified noncontrolled substances identified by the State Board of Pharmacy that are dispensed to residents in the State of Mississippi by licensed pharmacies, nonresident pharmacies, institutions and dispensing practitioners, regardless of dispenser location.

          (c)  The Board of Pharmacy shall report any activity it reasonably suspects may be fraudulent or illegal to the appropriate law enforcement agency or occupational licensing board and provide them with the relevant information obtained for further investigation.

          (d)  The program shall provide information regarding the potential inappropriate use of controlled substances and the specified noncontrolled substances to practitioners, pharmacists-in-charge and appropriate state agencies in order to prevent the inappropriate or illegal use of these controlled substances.  The specific purposes of the program shall be to:  be proactive in safeguarding public health and safety; support the legitimate use of controlled substances; facilitate and encourage the identification, intervention with and treatment of individuals addicted to controlled substances and specified noncontrolled drugs; identify and prevent drug diversion; provide assistance to those state and federal law enforcement and regulatory agencies investigating cases of drug diversion or other misuse; and inform the public and health care professionals of the use and abuse trends related to controlled substance and specified noncontrolled drugs.

          (e)  (i)  Access to collected data shall be confidential and not subject to the provisions of the federal Freedom of Information Act or the Mississippi Public Records Act.  Upon request, the State Board of Pharmacy shall provide collected information to:  pharmacists or practitioners who are properly registered with the State Board of Pharmacy and are authorized to prescribe or dispense controlled substances for the purpose of providing medical and pharmaceutical care for their patients; local, state and federal law enforcement officials engaged in the administration, investigation or enforcement of the laws governing illicit drug use; regulatory and licensing boards in this state; Division of Medicaid regarding Medicaid and Medicare Program recipients; judicial authorities under grand jury subpoena; an individual who requests the individual's own prescription monitoring information; and prescription monitoring programs in other states through mutual agreement adhering to State Board of Pharmacy policies.

              (ii)  The Director of the Mississippi Bureau of Narcotics, or his or her designee, shall have access to the Prescription Monitoring Program (PMP) database for the purpose of investigating the potential illegal acquisition, distribution, dispensing, prescribing or administering of the controlled and noncontrolled substances monitored by the program, subject to all legal restrictions on further dissemination of the information obtained.

              (iii)  The State Board of Pharmacy may also provide statistical data for research or educational purposes if the board determines the use of the data to be of significant benefit to public health and safety.  The board maintains the right to refuse any request for PMP data.

              (iv)  A pharmacist licensed by the Mississippi Board of Pharmacy must be a registered user of the PMP.  Failure of a pharmacist licensed by the Mississippi Board of Pharmacy to register as a user of the PMP is grounds for disciplinary action by the board.

              (v)  All licensed practitioners as defined under Section 73-21-73(ee) holding an active DEA number shall register as users of the PMP.

          (f)  The Prescription Monitoring Program through the Board of Pharmacy may:

              (i)  Establish the cost of administration, maintenance, and operation of the program and charge to like agencies a fee based on a formula to be determined by the board with collaboration and input from participating agencies; and

              (ii)  Assess charges for information and/or statistical data provided to agencies, institutions and individuals.  The amounts of those fees shall be set by the Executive Director of the Board of Pharmacy based on the recommendation of the Director of the PMP.

     All such fees collected shall be deposited into the special fund of the State Board of Pharmacy and used to support the operations of the PMP.

          (g)  A dispenser pharmacist or practitioner licensed to dispense controlled substances and specified noncontrolled substance drugs who knowingly fails to submit drug-monitoring information or knowingly submits incorrect dispensing information shall be subject to actions against the pharmacist's or practitioner's license, registrations or permit and/or an administrative penalty as provided in Sections 73-21-97 and 73-21-103.  Any misuse of the PMP is subject to penalties as provided in Sections 73-21-97 and 73-21-103.

          (h)  The Board of Pharmacy and the Prescription Monitoring Program shall be immune from civil liability arising from inaccuracy of any of the information submitted to the program.

          (i)  "Practitioner," as used in this section, shall include any person licensed, registered or otherwise permitted to distribute, dispense, prescribe or administer a controlled substance, as defined under Section 41-29-105(y), and any person defined as a "practitioner" under Section 73-21-73(ee).

          (j)  In addition to any funds appropriated by the Legislature, the State Board of Pharmacy may apply for any available grants and accept any gifts, grants or donations to assist in future development or in maintaining the program.

     (2)  In addition to receiving the dispensing information regarding controlled substances as provided in subsection (1) of this section, the State Board of Pharmacy shall receive and maintain in the Prescription Monitoring Program (a) the medical cannabis dispensing information that medical cannabis specialty pharmacies under the Mississippi Medical Cannabis Compassion Act are required to report to the PMP under the act, and (b) any other medical cannabis dispensing information that specialty pharmacies are required to report to the PMP.  The medical cannabis dispensing information reported by medical cannabis specialty pharmacies under the Mississippi Medical Cannabis Compassion Act shall not be considered to be a prescription for the purposes of the Mississippi Pharmacy Practice Act or the Uniform Controlled Substance Law.

     SECTION 36.  Section 73-25-29, Mississippi Code of 1972, is amended as follows:

     73-25-29.  The grounds for the nonissuance, suspension, revocation or restriction of a license or the denial of reinstatement or renewal of a license are:

          (1)  Habitual personal use of narcotic drugs, or any other drug having addiction-forming or addiction-sustaining liability.

          (2)  Habitual use of intoxicating liquors, or any beverage, to an extent which affects professional competency.

          (3)  Administering, dispensing or prescribing any narcotic drug, or any other drug having addiction-forming or addiction-sustaining liability otherwise than in the course of legitimate professional practice.

          (4)  Conviction of violation of any federal or state law regulating the possession, distribution or use of any narcotic drug or any drug considered a controlled substance under state or federal law, a certified copy of the conviction order or judgment rendered by the trial court being prima facie evidence thereof, notwithstanding the pendency of any appeal.

          (5)  Procuring, or attempting to procure, or aiding in, an abortion that is not medically indicated.

          (6)  Conviction of a felony or misdemeanor involving moral turpitude, a certified copy of the conviction order or judgment rendered by the trial court being prima facie evidence thereof, notwithstanding the pendency of any appeal.

          (7)  Obtaining or attempting to obtain a license by fraud or deception.

          (8)  Unprofessional conduct, which includes, but is not limited to:

              (a)  Practicing medicine under a false or assumed name or impersonating another practitioner, living or dead.

              (b)  Knowingly performing any act which in any way assists an unlicensed person to practice medicine.

              (c)  Making or willfully causing to be made any flamboyant claims concerning the licensee's professional excellence.

              (d)  Being guilty of any dishonorable or unethical conduct likely to deceive, defraud or harm the public.

              (e)  Obtaining a fee as personal compensation or gain from a person on fraudulent representation of a disease or injury condition generally considered incurable by competent medical authority in the light of current scientific knowledge and practice can be cured or offering, undertaking, attempting or agreeing to cure or treat the same by a secret method, which he or she refuses to divulge to the board upon request.

              (f)  Use of any false, fraudulent or forged statement or document, or the use of any fraudulent, deceitful, dishonest or immoral practice in connection with any of the licensing requirements, including the signing in his or her professional capacity any certificate that is known to be false at the time he or she makes or signs such certificate.

              (g)  Failing to identify a physician's school of practice in all professional uses of his or her name by use of his or her earned degree or a description of his or her school of practice.

          (9)  The refusal of a licensing authority of another state or jurisdiction to issue or renew a license, permit or certificate to practice medicine in that jurisdiction or the revocation, suspension or other restriction imposed on a license, permit or certificate issued by such licensing authority which prevents or restricts practice in that jurisdiction, a certified copy of the disciplinary order or action taken by the other state or jurisdiction being prima facie evidence thereof, notwithstanding the pendency of any appeal.

          (10)  Surrender of a license or authorization to practice medicine in another state or jurisdiction or surrender of membership on any medical staff or in any medical or professional association or society while under disciplinary investigation by any of those authorities or bodies for acts or conduct similar to acts or conduct which would constitute grounds for action as defined in this section.

          (11)  Final sanctions imposed by the United States Department of Health and Human Services, Office of Inspector General or any successor federal agency or office, based upon a finding of incompetency, gross misconduct or failure to meet professionally recognized standards of health care; a certified copy of the notice of final sanction being prima facie evidence thereof.  As used in this paragraph, the term "final sanction" means the written notice to a physician from the United States Department of Health and Human Services, Officer of Inspector General or any successor federal agency or office, which implements the exclusion.

          (12)  Failure to furnish the board, its investigators or representatives information legally requested by the board.

          (13)  Violation of any provision(s) of the Medical Practice Act or the rules and regulations of the board or of any order, stipulation or agreement with the board.

          (14)  Violation(s) of the provisions of Sections 41-121-1 through 41-121-9 relating to deceptive advertisement by health care practitioners.

          (15)  Performing or inducing an abortion on a woman in violation of any provision of Sections 41-41-131 through 41-41-145.

          (16)  Performing an abortion on a pregnant woman after determining that the unborn human individual that the pregnant woman is carrying has a detectable fetal heartbeat as provided in Section 41-41-34.1.

     In addition to the grounds specified above, the board shall be authorized to suspend the license of any licensee for being out of compliance with an order for support, as defined in Section 93-11-153.  The procedure for suspension of a license for being out of compliance with an order for support, and the procedure for the reissuance or reinstatement of a license suspended for that purpose, and the payment of any fees for the reissuance or reinstatement of a license suspended for that purpose, shall be governed by Section 93-11-157 or 93-11-163, as the case may be.  If there is any conflict between any provision of Section 93-11-157 or 93-11-163 and any provision of this chapter, the provisions of Section 93-11-157 or 93-11-163, as the case may be, shall control.

     A physician who provides a written certification as authorized under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder shall not be subject to any disciplinary action under this section solely due to providing the written certification and recommendation.

     SECTION 37.  Section 83-9-22, Mississippi Code of 1972, is amended as follows:

     83-9-22.  (1)  (a)  Notwithstanding any other provision of the law to the contrary, except as otherwise provided in subsection (3) of this section, no health coverage plan shall restrict coverage for medically appropriate treatment prescribed by a physician and agreed to by a fully informed insured, or if the insured lacks legal capacity to consent by a person who has legal authority to consent on his or her behalf, based on an insured's diagnosis with a terminal condition.  Refusing to pay for treatment rendered to an insured near the end of life that is consistent with best practices for treatment of a disease or condition, approved uses of a drug or device, or uses supported by peer reviewed medical literature, is a per se violation of this section.

          (b)  Violations of this section shall constitute an unfair trade practice and subject the violator to the penalties provided by law.

          (c)  As used in this section "terminal condition" means any aggressive malignancy, chronic end-stage cardiovascular or cerebral vascular disease, or any other disease, illness or condition which a physician diagnoses as terminal.

          (d)  As used in this section, a "health coverage plan" shall mean any hospital, health or medical expense insurance policy, hospital or medical service contract, employee welfare benefit plan, contract or agreement with a health maintenance organization or a preferred provider organization, health and accident insurance policy, or any other insurance contract of this type, including a group insurance plan and the State Health and Life Insurance Plan.

     (2)  (a)  Notwithstanding any other provision of the law to the contrary, no health benefit paid directly or indirectly with state funds, specifically Medicaid, shall restrict coverage for medically appropriate treatment prescribed by a physician and agreed to by a fully informed individual, or if the individual lacks legal capacity to consent by a person who has legal authority to consent on his or her behalf, based on an individual's diagnosis with a terminal condition.

          (b)  Refusing to pay for treatment rendered to an individual near the end of life that is consistent with best practices for treatment of a disease or condition, approved uses of a drug or device, or uses supported by peer reviewed medical literature, is a per se violation of this section.

          (c)  As used in this section "terminal condition" means any aggressive malignancy, chronic end-stage cardiovascular or cerebral vascular disease, or any other disease, illness or condition which a physician diagnoses as terminal.

     (3)  This section does not require a health coverage plan to cover and pay for the treatment of a person who is a registered qualifying patient for medical cannabis that is lawful under the Mississippi Medical Cannabis Compassion Act and in compliance with rules and regulations adopted thereunder.

     SECTION 38.  This act shall take effect and be in force from and after July 1, 2022.


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