Mr. Booker (for himself, Mr. Schmitt, Mr. King, Mr. Kennedy, Mr. Whitehouse, Mr. Marshall, Mr. Blumenthal, Mr. Paul, and Mr. Luján) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and Pensions
To require the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, to publish a final rule relating to nonclinical testing methods.
Eric Schmitt
(MO); Angus S. King Jr.
(ME); John Kennedy
(LA); Sheldon Whitehouse
(RI); Roger Marshall
(KS); Richard Blumenthal
(CT); Rand Paul
(KY); Ben Ray Lujan
(NM)
Citations are generated automatically from bibliographic data as a convenience and may not be complete or accurate.
Chicago
U.S. Congress. Senate. FDA Modernization Act 3.0. S. 355. 119th
Cong., 1st
sess., Introduced in Senate February 3, 2025. https://www.govinfo.gov/app/details/BILLS-119s355is.
APA
Congress, Senate (2025, February 3). FDA Modernization Act 3.0 (S. 355 (IS)). Retrieved from https://www.govinfo.gov/app/details/BILLS-119s355is.
MLA
United States, Congress, Senate. FDA Modernization Act 3.0. U.S. Government Publishing Office, https://www.govinfo.gov/app/details/BILLS-119s355is. 119th Congress, S. 355, Introduced in Senate 3 Feb. 2025.
Bluebook
S.355 - 119th Congress (2025-2026): FDA Modernization Act 3.0, S.355, 119th Cong. (2025), https://www.govinfo.gov/app/details/BILLS-119s355is.
