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1(d) Two members appointed for 4-year terms who represent the health care
2industry, including hospitals, physicians, pharmacies, and pharmacists. At least one
3of the members appointed under this paragraph shall be a licensed practitioner.
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(e) Two members appointed for 4-year terms who represent the interests of the
5public.
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6(2) A member appointed under sub. (1), except for a member appointed under
7sub. (1) (b), may not be an employee of, a board member of, or a consultant to a drug
8manufacturer or trade association for drug manufacturers.
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9(3) Any conflict of interest, including any financial or personal association, that
10has the potential to bias or has the appearance of biasing an individual's decision in
11matters related to the board or the conduct of the board's activities shall be
12considered and disclosed when appointing that individual to the board under sub.
13(1).
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14Section
80. Subchapter VI (title) of chapter 601 [precedes 601.78] of the
15statutes is created to read:
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CHAPTER 601
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SUBCHAPTER VI
18
Prescription drug
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affordability review board
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20Section
81. 601.78 of the statutes is created to read:
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21601.78 Definitions. In this subchapter:
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22(1) “Biologic” means a drug that is produced or distributed in accordance with
23a biologics license application approved under
21 CFR 601.20.
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24(2) “Biosimilar” means a drug that is produced or distributed in accordance
25with a biologics license application approved under
42 USC 262 (k) (3).
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1(3) “Board” means the prescription drug affordability review board established
2under s. 15.735 (1).
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3(4) “Brand name drug” means a drug that is produced or distributed in
4accordance with an original new drug application approved under
21 USC 355 (c),
5other than an authorized generic drug, as defined in
42 CFR 447.502.
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6(5) “Financial benefit” includes an honorarium, fee, stock, the value of the stock
7holdings of a member of the board or any immediate family member, and any direct
8financial benefit deriving from the finding of a review conducted under s. 601.79.
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9(6) “Generic drug” means any of the following:
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(a) A retail drug that is marketed or distributed in accordance with an
11abbreviated new drug application approved under
21 USC 355 (j).
SB70-AA3,84,1212(b) An authorized generic drug, as defined in
42 CFR 447.502.
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(c) A drug that entered the market prior to 1962 and was not originally
14marketed under a new drug application.
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15(7) “Immediate family member” means a spouse, grandparent, parent, sibling,
16child, stepchild, or grandchild or the spouse of a grandparent, parent, sibling, child,
17stepchild, or grandchild.
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18(8) “Manufacturer” means an entity that does all of the following:
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(a) Engages in the manufacture of a prescription drug product or enters into
20a lease with another manufacturer to market and distribute a prescription drug
21product under the entity's own name.
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(b) Sets or changes the wholesale acquisition cost of the prescription drug
23product described in par. (a).
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24(9) “Pharmacy benefit manager” has the meaning given in s. 632.865 (1) (c).
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1(10) “Prescription drug product” means a brand name drug, a generic drug, a
2biologic, or a biosimilar.
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3Section
82. 601.785 of the statutes is created to read:
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4601.785 Prescription drug affordability review board. (1) Mission. The
5purpose of the board is to protect state residents, the state, local governments, health
6plans, health care providers, pharmacies licensed in this state, and other
7stakeholders of the health care system in this state from the high costs of prescription
8drug products.
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9(2) Powers and duties. (a) The board shall do all of the following:
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1. Meet in open session at least 4 times per year to review prescription drug
11product pricing information, except that the chair may cancel or postpone a meeting
12if there is no business to transact.