Bill Amendment: IL SB3322 | 2025-2026 | 104th General Assembly
NOTE: For additional amemendments please see the Bill Drafting List
Bill Title: MENTAL HEALTH REHABILITATION
Status: 2026-06-29 - Sent to the Governor [SB3322 Detail]
Download: Illinois-2025-SB3322-House_Amendment_003.html
Bill Title: MENTAL HEALTH REHABILITATION
Status: 2026-06-29 - Sent to the Governor [SB3322 Detail]
Download: Illinois-2025-SB3322-House_Amendment_003.html
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| 1 | AMENDMENT TO SENATE BILL 3322 | ||||||
| 2 | AMENDMENT NO. ______. Amend Senate Bill 3322, AS AMENDED, | ||||||
| 3 | by replacing everything after the enacting clause with the | ||||||
| 4 | following: | ||||||
| 5 | "Section 5. The Illinois Controlled Substances Act is | ||||||
| 6 | amended by changing Section 201 as follows: | ||||||
| 7 | (720 ILCS 570/201) (from Ch. 56 1/2, par. 1201) | ||||||
| 8 | Sec. 201. (a) The Department shall carry out the | ||||||
| 9 | provisions of this Article. The Department or its successor | ||||||
| 10 | agency may, by administrative rule, add additional substances | ||||||
| 11 | to or delete or reschedule all controlled substances in the | ||||||
| 12 | Schedules of Sections 204, 206, 208, 210 and 212 of this Act. | ||||||
| 13 | In making a determination regarding the addition, deletion, or | ||||||
| 14 | rescheduling of a substance, the Department shall consider the | ||||||
| 15 | following: | ||||||
| 16 | (1) the actual or relative potential for misuse; | ||||||
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| 1 | (2) the scientific evidence of its pharmacological | ||||||
| 2 | effect, if known; | ||||||
| 3 | (3) the state of current scientific knowledge | ||||||
| 4 | regarding the substance; | ||||||
| 5 | (4) the history and current pattern of misuse; | ||||||
| 6 | (5) the scope, duration, and significance of misuse; | ||||||
| 7 | (6) the risk to the public health; | ||||||
| 8 | (7) the potential of the substance to produce | ||||||
| 9 | psychological or physiological dependence or a substance | ||||||
| 10 | use disorder; | ||||||
| 11 | (8) whether the substance is an immediate precursor of | ||||||
| 12 | a substance already controlled under this Article; | ||||||
| 13 | (9) the immediate harmful effect in terms of | ||||||
| 14 | potentially fatal dosage; and | ||||||
| 15 | (10) the long-range effects in terms of permanent | ||||||
| 16 | health impairment. | ||||||
| 17 | (b) (Blank). | ||||||
| 18 | (c) (Blank). | ||||||
| 19 | (d) If any substance is scheduled, rescheduled, or deleted | ||||||
| 20 | as a controlled substance under Federal law and notice thereof | ||||||
| 21 | is given to the Department, the Department shall similarly | ||||||
| 22 | control the substance under this Act after the expiration of | ||||||
| 23 | 30 days from publication in the Federal Register of a final | ||||||
| 24 | order scheduling a substance as a controlled substance or | ||||||
| 25 | rescheduling or deleting a substance. If the Department does | ||||||
| 26 | not take action within 30 days, at the conclusion of the 30-day | ||||||
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| 1 | period the substance shall be considered scheduled, | ||||||
| 2 | rescheduled, or deleted in the same manner as the federal law, | ||||||
| 3 | unless within that 30-day 30 day period the Department | ||||||
| 4 | objects, or a party adversely affected files with the | ||||||
| 5 | Department substantial written objections objecting to | ||||||
| 6 | inclusion, rescheduling, or deletion. In that case, the | ||||||
| 7 | Department shall publish the reasons for objection or the | ||||||
| 8 | substantial written objections and afford all interested | ||||||
| 9 | parties an opportunity to be heard in a public hearing to be | ||||||
| 10 | held no later than 45 days after the statement of objection. | ||||||
| 11 | After At the public conclusion of the hearing, the Department | ||||||
| 12 | shall publish its decision within 14 days of the conclusion of | ||||||
| 13 | the public hearing, by means of a rule, which shall be final | ||||||
| 14 | unless altered by statute. Upon publication of objections by | ||||||
| 15 | the Department, similar control under this Act whether by | ||||||
| 16 | inclusion, rescheduling or deletion is stayed until the | ||||||
| 17 | Department publishes its ruling. | ||||||
| 18 | (e) (Blank). | ||||||
| 19 | (f) (Blank). | ||||||
| 20 | (g) Authority to control under this Section does not | ||||||
| 21 | extend to distilled spirits, wine, malt beverages, or tobacco | ||||||
| 22 | as those terms are defined or used in the Liquor Control Act of | ||||||
| 23 | 1934 and the Tobacco Products Tax Act of 1995. | ||||||
| 24 | (h) Persons registered with the Drug Enforcement | ||||||
| 25 | Administration to manufacture or distribute controlled | ||||||
| 26 | substances shall maintain adequate security and provide | ||||||
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| 1 | effective controls and procedures to guard against theft and | ||||||
| 2 | diversion, but shall not otherwise be required to meet the | ||||||
| 3 | physical security control requirements (such as cage or vault) | ||||||
| 4 | for Schedule V controlled substances containing | ||||||
| 5 | pseudoephedrine or Schedule II controlled substances | ||||||
| 6 | containing dextromethorphan. | ||||||
| 7 | (Source: P.A. 103-881, eff. 1-1-25.) | ||||||
| 8 | Section 99. Effective date. This Act takes effect upon | ||||||
| 9 | becoming law.". | ||||||
