Bill Text: NY S03217 | 2009-2010 | General Assembly | Introduced


Bill Title: Enacts the New York state pharmaceutical drug manufacturer and wholesaler disclosure act; requires pharmaceutical drug manufacturers and wholesalers to annually report to the New York department of health, for disclosure to the general public, all of its gifts to health care practitioners that prescribe drugs when such gifts have a value of seventy-five dollars or more; authorizes the commissioner of health to impose penalties and promulgate necessary rules and regulations.

Sponsorship: Strong Partisan Bill (Republican 12-1)

Status: (Introduced - Dead) 2010-01-06 - REFERRED TO HEALTH [S03217 Detail]

Download: New_York-2009-S03217-Introduced.html
                           S T A T E   O F   N E W   Y O R K
       ________________________________________________________________________
                                         3217
                              2009-2010 Regular Sessions
                                   I N  S E N A T E
                                    March 12, 2009
                                      ___________
       Introduced  by  Sens.  MAZIARZ,  ALESI, BONACIC, DeFRANCISCO, FUSCHILLO,
         GOLDEN, GRIFFO, LAVALLE, MORAHAN, OPPENHEIMER,  PADAVAN,  RANZENHOFER,
         SALAND  --  read  twice  and  ordered  printed, and when printed to be
         committed to the Committee on Health
       AN ACT to amend the public health law,  in  relation  to  disclosure  of
         certain  gifts provided by drug manufacturers or wholesalers to health
         care providers
         THE PEOPLE OF THE STATE OF NEW YORK, REPRESENTED IN SENATE AND  ASSEM-
       BLY, DO ENACT AS FOLLOWS:
    1    Section  1.  Article 2 of the public health law is amended by adding a
    2  new title 6 to read as follows:
    3                                  TITLE VI
    4             NEW YORK STATE PHARMACEUTICAL DRUG MANUFACTURER AND
    5                          WHOLESALER DISCLOSURE ACT
    6  SECTION 266.   LEGISLATIVE INTENT.
    7          266-A. DEFINITIONS.
    8          266-B. DISCLOSURE REQUIREMENTS.
    9          266-C. ANNUAL CONSUMER GUIDE ON PHARMACEUTICAL DRUG MANUFACTURER
   10                   AND WHOLESALER GIFTS TO HEALTH CARE PROVIDERS.
   11          266-D. PENALTIES.
   12          266-E. RULES AND REGULATIONS.
   13    S 266. LEGISLATIVE INTENT.   THE LEGISLATURE FINDS THAT  THE  COST  OF
   14  PRESCRIPTION DRUGS IN THE UNITED STATES HAS GROWN DRAMATICALLY.  ACCORD-
   15  ING  TO THE CENTERS FOR DISEASE CONTROL, SPENDING ON RETAIL PRESCRIPTION
   16  DRUGS IN THE UNITED  STATES  MORE  THAN  TRIPLED  FROM  FIFTEEN  BILLION
   17  DOLLARS  IN  NINETEEN  HUNDRED  EIGHTY-TWO  TO  FORTY-EIGHT  BILLION TWO
   18  HUNDRED MILLION DOLLARS IN NINETEEN HUNDRED NINETY-TWO, THEN  MORE  THAN
   19  TRIPLED  AGAIN  TO  ONE  HUNDRED  SIXTY-TWO BILLION FOUR HUNDRED MILLION
   20  DOLLARS IN TWO THOUSAND TWO. IN PER CAPITA  TERMS,  RETAIL  PRESCRIPTION
   21  DRUGS  SPENDING  INCREASED  FROM  SIXTY-FOUR DOLLARS IN NINETEEN HUNDRED
        EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets
                             [ ] is old law to be omitted.
                                                                  LBD06145-01-9
       S. 3217                             2
    1  EIGHTY-TWO TO FIVE HUNDRED SIXTY-NINE DOLLARS IN TWO THOUSAND TWO.    IN
    2  TWO  THOUSAND  FIVE,  SPENDING  ON  PHARMACEUTICALS  ROSE TO TWO HUNDRED
    3  FIFTY-ONE BILLION EIGHT HUNDRED MILLION DOLLARS.  WHILE THE AVAILABILITY
    4  OF  USEFUL  NEW DRUGS TO TREAT CHRONIC CONDITIONS SUCH AS HEART DISEASE,
    5  HYPERTENSION AND DEPRESSION ACCOUNTS FOR MUCH OF THE INCREASED SPENDING,
    6  THERE IS WIDESPREAD CONCERN ABOUT THE  IMPACT  AGGRESSIVE  MARKETING  BY
    7  DRUG MANUFACTURERS AND WHOLESALERS HAS HAD ON DRUG COSTS AND PRESCRIBING
    8  PATTERNS.  IN  ADDITION  TO  THE  EXPLOSIVE GROWTH IN DIRECT-TO-CONSUMER
    9  ADVERTISING, THESE MARKETING EFFORTS ARE OFTEN DIRECTED AT  HEALTH  CARE
   10  PROVIDERS  AND  INCLUDE GIFTS, PARAPHERNALIA, TRIPS AND TRAVEL, FOOD AND
   11  ENTERTAINMENT. A COMPETITIVE  MEDIA  REPORTING  STUDY  FOUND  THAT  DRUG
   12  COMPANIES  PROVIDED  SEVEN  BILLION TWO HUNDRED MILLION DOLLARS WORTH OF
   13  FREE SAMPLES TO PHYSICIANS' OFFICES  IN  NINETEEN  HUNDRED  NINETY-NINE.
   14  THE  DRUG  INDUSTRY  SPONSORED MORE THAN THREE HUNDRED FOURTEEN THOUSAND
   15  PHYSICIAN "EVENTS" IN TWO THOUSAND ONE, RANGING FROM CATERED LUNCHES  IN
   16  HOSPITAL  CONFERENCE ROOMS TO WEEKEND GETAWAYS AT RESORTS, NEARLY DOUBLE
   17  THE NUMBER FOUR YEARS EARLIER.  DRUG  COMPANIES  SPENT  SOME  TWENTY-TWO
   18  BILLION  DOLLARS  IN  MARKETING IN TWO THOUSAND THREE.  ACCORDING TO THE
   19  JOURNAL OF THE AMERICAN MEDICAL  ASSOCIATION,  NINETY  PERCENT  OF  DRUG
   20  COMPANY  MARKETING IS DIRECTED AT PHYSICIANS.  ESTEEMED MEDICAL PUBLICA-
   21  TIONS SUCH AS THE JOURNAL OF THE AMERICAN MEDICAL  ASSOCIATION  AND  THE
   22  BRITISH  MEDICAL  JOURNAL  PRODUCED STUDIES THAT SUGGEST THESE MARKETING
   23  ACTIVITIES DO INFLUENCE HEALTH CARE PROVIDERS' DECISIONS ON PRESCRIPTION
   24  DRUGS, AND IN WAYS THAT ARE NOT THE BEST FOR PATIENTS OR THE HEALTH CARE
   25  SYSTEM ITSELF. THE LEGISLATURE RECOGNIZES THAT  DRUG  MANUFACTURERS  AND
   26  WHOLESALERS  ARE FREE TO USE ANY LEGAL SALES AND MARKETING TECHNIQUES TO
   27  PROMOTE THEIR PRODUCTS. BUT THE LEGISLATURE ALSO FINDS THAT THE  CONSUM-
   28  ERS HAVE A RIGHT TO KNOW WHAT GIFTS, IF ANY, THEIR HEALTH CARE PROVIDERS
   29  ARE  RECEIVING  FROM  MANUFACTURERS  AND WHOLESALERS, IN ORDER THAT THEY
   30  MIGHT  MAKE  INFORMED   AND   COST-EFFECTIVE   DECISIONS   ABOUT   THEIR
   31  PRESCRIPTION DRUG EXPENDITURES.
   32    S 266-A. DEFINITIONS. AS USED IN THIS TITLE, THE FOLLOWING TERMS SHALL
   33  HAVE THE FOLLOWING MEANINGS:
   34    1.  "APPROVED  CLINICAL  TRIAL"  MEANS  A CLINICAL TRIAL THAT HAS BEEN
   35  APPROVED BY THE U.S. FOOD AND DRUG  ADMINISTRATION  (FDA)  OR  HAS  BEEN
   36  APPROVED  BY  A  DULY CONSTITUTED INSTITUTIONAL REVIEW BOARD (IRB) AFTER
   37  REVIEWING AND  EVALUATING  IT  IN  ACCORDANCE  WITH  THE  HUMAN  SUBJECT
   38  PROTECTION  STANDARDS SET FORTH AT 21 C.F.R. PART 50, 45 C.F.R. PART 46,
   39  OR AN EQUIVALENT SET OF STANDARDS OF ANOTHER FEDERAL AGENCY.
   40    2. "BONA FIDE CLINICAL TRIAL" MEANS AN APPROVED  CLINICAL  TRIAL  THAT
   41  CONSTITUTES  "RESEARCH"  AS  THAT  TERM IS DEFINED IN 45 C.F.R. S 46.102
   42  WHEN THE RESULTS OF THE RESEARCH CAN BE PUBLISHED FREELY BY THE INVESTI-
   43  GATOR AND REASONABLY CAN BE CONSIDERED TO BE OF INTEREST  TO  SCIENTISTS
   44  OR MEDICAL PRACTITIONERS WORKING IN THE PARTICULAR FIELD OF INQUIRY.
   45    3.  "CLINICAL  TRIAL" MEANS ANY STUDY ASSESSING THE SAFETY OR EFFICACY
   46  OF DRUGS ADMINISTERED ALONE OR IN COMBINATION WITH OTHER DRUGS OR  OTHER
   47  THERAPIES,  OR  ASSESSING  THE  RELATIVE  SAFETY OR EFFICACY OF DRUGS IN
   48  COMPARISON WITH OTHER DRUGS OR OTHER THERAPIES.
   49    4. "DRUGS" SHALL HAVE THE SAME MEANING AS  SET  FORTH  IN  SUBDIVISION
   50  SEVEN OF SECTION SIX THOUSAND EIGHT HUNDRED TWO OF THE EDUCATION LAW.
   51    5.  "HEALTH  CARE PROVIDER" MEANS ANY PHYSICIAN OR OTHER PERSON WHO IS
   52  LEGALLY AUTHORIZED TO PRESCRIBE DRUGS.
   53    6. "PHARMACEUTICAL DRUG MANUFACTURER" MEANS A  PERSON  WHO  COMPOUNDS,
   54  MIXES,  PREPARES, PRODUCES AND BOTTLES OR PACKS DRUGS FOR THE PURPOSE OF
   55  DISTRIBUTING OR SELLING TO PHARMACIES OR TO OTHER CHANNELS  OF  DISTRIB-
   56  UTION.
       S. 3217                             3
    1    7. "PHARMACEUTICAL DRUG WHOLESALER" MEANS A PERSON WHOSE PRIMARY BUSI-
    2  NESS  PURPOSE  IS  TO  BOTTLE, PACK OR PURCHASE DRUGS FOR THE PURPOSE OF
    3  SELLING OR RESELLING TO PHARMACIES OR TO OTHER CHANNELS AS  PROVIDED  IN
    4  THIS TITLE.
    5    8.  "PHARMACY" SHALL HAVE THE SAME MEANING AS SET FORTH IN SUBDIVISION
    6  ONE OF SECTION SIX THOUSAND EIGHT HUNDRED TWO OF THE EDUCATION LAW.
    7    9. "UNRESTRICTED GRANT" MEANS ANY GIFT,  PAYMENT,  SUBSIDY,  OR  OTHER
    8  ECONOMIC  BENEFIT  TO  AN  EDUCATIONAL INSTITUTION, PROFESSIONAL ASSOCI-
    9  ATION, HEALTH CARE FACILITY,  OR  GOVERNMENTAL  ENTITY  WHICH  DOES  NOT
   10  IMPOSE  ANY  RESTRICTIONS  ON  THE  USE  OF THE GRANT, SUCH AS FAVORABLE
   11  TREATMENT OF A CERTAIN PRODUCT OR AN ABILITY OF THE MARKETER TO  CONTROL
   12  OR INFLUENCE THE PLANNING, CONTENT, OR EXECUTION OF THE EDUCATION ACTIV-
   13  ITY.
   14    S  266-B. DISCLOSURE REQUIREMENTS. 1. ANY PHARMACEUTICAL DRUG MANUFAC-
   15  TURER OR PHARMACEUTICAL DRUG WHOLESALER, INCLUDING ANY EMPLOYEE OR AGENT
   16  OF SUCH MANUFACTURER OR WHOLESALER, THAT MAKES ANY GIFT WHETHER  IN  THE
   17  FORM  OF MONEY, SERVICE, LOAN, TRAVEL, ENTERTAINMENT, HOSPITALITY, THING
   18  OR PROMISE, OR IN ANY OTHER FORM, TO A HEALTH CARE PROVIDER SHALL REPORT
   19  THE GIFT TO THE COMMISSIONER IN THE MANNER SET FORTH IN SUBDIVISION  TWO
   20  OF THIS SECTION.
   21    2.  ANY PHARMACEUTICAL DRUG MANUFACTURER OR PHARMACEUTICAL DRUG WHOLE-
   22  SALER WHO MAKES AT LEAST ONE GIFT UNDER SUBDIVISION ONE OF THIS  SECTION
   23  SHALL  FILE  WITH  THE  COMMISSIONER AN ANNUAL REPORT, DUE NO LATER THAN
   24  JUNE FIRST OF EACH YEAR, BEGINNING IN TWO THOUSAND ELEVEN, OF ALL  GIFTS
   25  MADE BY THE MANUFACTURER OR WHOLESALER TO HEALTH CARE PROVIDERS.
   26    3.  SUCH  ANNUAL REPORT SHALL CONTAIN: (A) THE NAME, ADDRESS AND TELE-
   27  PHONE NUMBER OF THE PHARMACEUTICAL DRUG MANUFACTURER OR WHOLESALER;  (B)
   28  AN  ITEMIZED  LIST  CONTAINING  A DESCRIPTION OF EACH GIFT FALLING UNDER
   29  SUBDIVISION ONE OF THIS SECTION AND  THE  NAME,  ADDRESS  AND  TELEPHONE
   30  NUMBER OF THE HEALTH CARE PROVIDER WHO RECEIVED EACH GIFT; (C) THE MONE-
   31  TARY VALUE OF EACH GIFT; AND (D) SUCH OTHER INFORMATION AS DEEMED NECES-
   32  SARY BY THE COMMISSIONER FOR COMPLIANCE WITH THIS ARTICLE.
   33    4. THE FOLLOWING SHALL BE EXEMPT FROM DISCLOSURE:
   34    (A)  THE  PAYMENT  OF  REASONABLE  COMPENSATION  AND  REIMBURSEMENT OF
   35  EXPENSES IN CONNECTION WITH BONA FIDE CLINICAL TRIALS;
   36    (B) ANY GIFT THE VALUE OF WHICH IS LESS THAN SEVENTY-FIVE DOLLARS;
   37    (C) SCHOLARSHIP OR OTHER SUPPORT FOR MEDICAL STUDENTS,  RESIDENTS  AND
   38  FELLOWS  TO ATTEND A SIGNIFICANT EDUCATIONAL, SCIENTIFIC, OR POLICY-MAK-
   39  ING CONFERENCE OF A NATIONAL, REGIONAL, OR SPECIALTY  MEDICAL  OR  OTHER
   40  PROFESSIONAL  ASSOCIATION  IF  THE RECIPIENT OF THE SCHOLARSHIP OR OTHER
   41  SUPPORT IS SELECTED BY THE ASSOCIATION;
   42    (D) UNRESTRICTED GRANTS FOR CONTINUING MEDICAL EDUCATION PROGRAMS;
   43    (E) PRESCRIPTION DRUG REBATES AND DISCOUNTS; AND
   44    (F) FREE SAMPLES OF DRUGS.
   45    S 266-C. ANNUAL CONSUMER GUIDE ON PHARMACEUTICAL DRUG MANUFACTURER AND
   46  WHOLESALER GIFTS TO HEALTH CARE PROVIDERS. 1. NO  LATER  THAN  SEPTEMBER
   47  FIRST  OF  EACH YEAR, BEGINNING IN TWO THOUSAND ELEVEN, THE COMMISSIONER
   48  SHALL PUBLISH AND MAKE AVAILABLE,  FREE  OF  CHARGE  TO  THE  PUBLIC,  A
   49  CONSUMER  GUIDE  ON  GIFTS PROVIDED BY PHARMACEUTICAL DRUG MANUFACTURERS
   50  AND WHOLESALERS TO HEALTH CARE PROVIDERS. SUCH GUIDE SHALL  CONTAIN  ALL
   51  OF THE INFORMATION PROVIDED IN THE ANNUAL REPORT REQUIRED BY SECTION TWO
   52  HUNDRED  SIXTY-SIX-B  OF THIS TITLE AND THE INFORMATION SHALL BE WRITTEN
   53  IN PLAIN LANGUAGE IN A CLEAR AND UNDERSTANDABLE FORMAT.
   54    2. THE COMMISSIONER SHALL PROVIDE FOR THE  ADEQUATE  DISTRIBUTION  AND
   55  AVAILABILITY  OF  THE CONSUMER GUIDE ON PHARMACEUTICAL DRUG MANUFACTURER
   56  AND WHOLESALER GIFTS TO HEALTH CARE PROVIDERS.   APPROPRIATE  COPIES  OF
       S. 3217                             4
    1  THE  GUIDE SHALL BE TRANSMITTED TO THE OFFICE FOR THE AGING FOR DISTRIB-
    2  UTION AT EVERY OFFICE FOR THE AGING IN THE STATE, TO EVERY COUNTY OFFICE
    3  FOR THE AGING IN THE STATE AND TO  THE  COMMISSIONER  OF  EDUCATION  FOR
    4  DISTRIBUTION  TO  EVERY  PUBLIC LIBRARY IN THE STATE WHERE COPIES OF THE
    5  GUIDE SHALL BE MADE AVAILABLE FREE OF CHARGE TO THE PUBLIC. THE  COMMIS-
    6  SIONER SHALL ALSO POST THE GUIDE ON THE DEPARTMENT'S INTERNET WEBSITE.
    7    S  266-D.  PENALTIES.   1. THE COMMISSIONER MAY IMPOSE A CIVIL PENALTY
    8  FOR FAILURE TO FILE A TIMELY REPORT AS REQUIRED BY SECTION  TWO  HUNDRED
    9  SIXTY-SIX-B  OF  THIS TITLE IN AN AMOUNT UP TO FIFTY DOLLARS A DAY UNTIL
   10  SUCH REPORT IS FILED OR THREE THOUSAND DOLLARS, WHICHEVER IS LESS.
   11    2. ANY PERSON WHO VIOLATES ANY OTHER PROVISION OF THIS TITLE SHALL  BE
   12  SUBJECT  TO  A  CIVIL  PENALTY IN AN AMOUNT NOT TO EXCEED THREE THOUSAND
   13  DOLLARS FOR EACH VIOLATION. THE COMMISSIONER IS AUTHORIZED TO ASSESS THE
   14  CIVIL PENALTY UNDER THIS SECTION PURSUANT  TO  SECTION  TWELVE  OF  THIS
   15  CHAPTER.
   16    S  266-E.  RULES  AND  REGULATIONS.  THE COMMISSIONER IS AUTHORIZED TO
   17  PROMULGATE RULES AND REGULATIONS AS DEEMED NECESSARY TO  CARRY  OUT  AND
   18  ENFORCE THE PROVISIONS OF THIS TITLE.
   19    S  2. This act shall take effect on the first of January next succeed-
   20  ing the date on which it shall have become a law.
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