SB70-AA3,84,8 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.
SB70-AA3,84,9 9(6) “Generic drug” means any of the following:
SB70-AA3,84,1110 (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.
SB70-AA3,84,1413 (c) A drug that entered the market prior to 1962 and was not originally
14marketed under a new drug application.
SB70-AA3,84,17 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.
SB70-AA3,84,18 18(8) “Manufacturer” means an entity that does all of the following:
SB70-AA3,84,2119 (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.
SB70-AA3,84,2322 (b) Sets or changes the wholesale acquisition cost of the prescription drug
23product described in par. (a).
SB70-AA3,84,24 24(9) “Pharmacy benefit manager” has the meaning given in s. 632.865 (1) (c).
SB70-AA3,85,2
1(10) “Prescription drug product” means a brand name drug, a generic drug, a
2biologic, or a biosimilar.
SB70-AA3,82 3Section 82. 601.785 of the statutes is created to read:
SB70-AA3,85,8 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.
SB70-AA3,85,9 9(2) Powers and duties. (a) The board shall do all of the following:
SB70-AA3,85,1210 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.
SB70-AA3,85,1413 2. To the extent practicable, access and assess pricing information for
14prescription drug products by doing all of the following:
SB70-AA3,85,1715 a. Accessing and assessing information from other states by entering into
16memoranda of understanding with other states to which manufacturers report
17pricing information.
SB70-AA3,85,1818 b. Assessing spending for specific prescription drug products in this state.
SB70-AA3,85,1919 c. Accessing other available pricing information.
SB70-AA3,85,2020 (b) The board may do any of the following:
SB70-AA3,85,2121 1. Promulgate rules for the administration of this subchapter.
SB70-AA3,86,222 2. Enter into a contract with an independent 3rd party for any service
23necessary to carry out the powers and duties of the board. Unless written permission
24is granted by the board, any person with whom the board contracts may not release,

1publish, or otherwise use any information to which the person has access under the
2contract.
SB70-AA3,86,53 (c) The board shall establish and maintain a website to provide public notices
4and make meeting materials available under sub. (3) (a) and to disclose conflicts of
5interest under sub. (4) (d).
SB70-AA3,86,9 6(3) Meeting requirements. (a) Pursuant to s. 19.84, the board shall provide
7public notice of each board meeting at least 2 weeks prior to the meeting and shall
8make the materials for each meeting publicly available at least one week prior to the
9meeting.
SB70-AA3,86,1210 (b) Notwithstanding s. 19.84 (2), the board shall provide an opportunity for
11public comment at each open meeting and shall provide the public with the
12opportunity to provide written comments on pending decisions of the board.
SB70-AA3,86,1513 (c) Notwithstanding subch. V of ch. 19, any portion of a meeting of the board
14concerning proprietary data and information shall be conducted in closed session
15and shall in all respects remain confidential.
SB70-AA3,86,1716 (d) The board may allow expert testimony at any meeting, including when the
17board meets in closed session.
SB70-AA3,86,21 18(4) Conflicts of interest. (a) A member of the board shall recuse himself or
19herself from a decision by the board relating to a prescription drug product if the
20member or an immediate family member has received or could receive any of the
21following:
SB70-AA3,86,2322 1. A direct financial benefit deriving from a determination, or a finding of a
23study or review, by the board relating to the prescription drug product.