Bill
Cannabinoid Product Board Membership Amendments
- Number
- H.B. 25 (2018GS)
- Sponsor
- Rep. Daw, B.
- Final action
- Governor Signed 3/16/2018
- Outcome
- Became law — signed by Gov. Gary R. Herbert
Summary
This bill amends provisions related to the Cannabinoid Product Board.
What it does
- This bill:
- amends the required composition of the Cannabinoid Product Board; and
- amends the duties of the Cannabinoid Product Board to include review of expanded cannabinoid products.
Every vote on this bill
1/25/2018House/ passed 3rd reading
Senate Secretary
70 0 5YEA1/30/2018Senate Comm - Favorable Recommendation
Senate Health and Human Services Committee
6 0 2not eligible / no record2/1/2018Senate/ circled
Senate 2nd Reading Calendar
Voice votenot eligible / no record2/7/2018Senate/ uncircled
Senate 2nd Reading Calendar
Voice votenot eligible / no record2/7/2018Senate/ passed 2nd reading
Senate 3rd Reading Calendar
23 1 5not eligible / no record3/6/2018Senate/ passed 3rd reading
Senate President
25 0 4not eligible / no recordBill text
introduced version · official source
CANNABINOID PRODUCT BOARD MEMBERSHIP AMENDMENTS GENERAL SESSION STATE OF UTAH Chief Sponsor: Brad M. Daw Senate Sponsor: Evan J. Vickers LONG TITLE Committee Note: The Health and Human Services Interim Committee recommended this bill. General Description: This bill amends provisions related to the Cannabinoid Product Board. Highlighted Provisions: This bill: ▸ amends the required composition of the Cannabinoid Product Board; and ▸ amends the duties of the Cannabinoid Product Board to include review of expanded cannabinoid products. Money Appropriated in this Bill: None Other Special Clauses: None Utah Code Sections Affected: AMENDS: 26-61-201 , as enacted by Laws of Utah 2017, Chapter 398 26-61-202 , as enacted by Laws of Utah 2017, Chapter 398 Be it enacted by the Legislature of the state of Utah: Section 1. Section 26-61-201 is amended to read: 26-61-201. Cannabinoid Product Board. (1) There is created the Cannabinoid Product Board within the department. (2) The department shall appoint, in consultation with a professional association based in the state that represents physicians, seven members to the Cannabinoid Product Board as follows: (a) three individuals who are medical research professionals; and (b) four physicians. (3) The department shall [ appoint board members under Subsection (2) such ] ensure that [ three ] at least one of the board members [ are members ] appointed under Subsection (2) is a member of the Controlled Substances Advisory Committee created in Section 58-38a-201 . (4) (a) Four of the board members appointed under Subsection (2) shall serve an initial term of two years and three of the board members appointed under Subsection (2) shall serve an initial term of four years. (b) Successor board members shall each serve a term of four years. (5) The department may remove a board member without cause. (6) The board shall nominate a board member to serve as chairperson of the board by a majority vote of the board members. (7) The board shall meet as often as necessary to accomplish the duties assigned to the board under this chapter. (8) Each board member, including the chair, has one vote. (9) (a) A majority of board members constitutes a quorum. (b) A vote of a majority of the quorum at any board meeting is necessary to take action on behalf of the board. (10) A board member may not receive compensation for the member's service on the board, but may, in accordance with rules adopted by the board in accordance with Title 63G, Chapter 3, Utah Administrative Rulemaking Act, receive: (a) per diem at the rate established under Section 63A-3-106 ; and (b) travel expenses at the rate established under Section 63A-3-107 . Section 2. Section 26-61-202 is amended to read: 26-61-202. Cannabinoid Product Board -- Duties. (1) The board shall review any available research related to the human use of a cannabinoid product or an expanded cannabinoid product that: (a) was conducted under a study approved by an IRB; or (b) was conducted or approved by the federal government. (2) Based on the research described in Subsection (1), the board shall evaluate the safety , risks, and efficacy of cannabinoid products and expanded cannabinoid products , including: (a) medical conditions that respond to cannabinoid products and expanded cannabinoid products ; (b) cannabinoid dosage amounts and medical dosage forms; and (c) interaction of cannabinoid products and expanded cannabinoid products with other treatments. (3) Based on the board's evaluation under Subsection (2), the board shall develop guidelines for a physician recommending treatment with a cannabinoid product or an expanded cannabinoid product that includes a list of medical conditions, if any, that the board determines are appropriate for treatment with a cannabinoid product or an expanded cannabinoid product . (4) The board shall submit the guidelines described in Subsection (3) to: (a) the director of the Division of Occupational and Professional Licensing; and (b) the Health and Human Services Interim Committee. (5) The board shall report the board's findings before November 1 of each year to the Health and Human Services Interim Committee. Legislative Review Note Office of Legislative Research and General Counsel