Mr. Carter of Georgia (for himself, Ms. Barragán, Mr. Buchanan, Ms. DeLauro, Mrs. Harshbarger, and Mr. Carter of Louisiana) introduced the following bill; which was referred to the Committee on Energy and Commerce
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.
Citations are generated automatically from bibliographic data as a convenience and may not be complete or accurate.
Chicago
U.S. Congress. House. FDA Modernization Act 3.0. H.R. 2821. 119th
Cong., 1st
sess., Introduced in House April 10, 2025. https://www.govinfo.gov/app/details/BILLS-119hr2821ih.
APA
Congress, House of Representatives (2025, April 10). FDA Modernization Act 3.0 (H.R. 2821 (IH)). Retrieved from https://www.govinfo.gov/app/details/BILLS-119hr2821ih.
MLA
United States, Congress, House of Representatives. FDA Modernization Act 3.0. U.S. Government Publishing Office, https://www.govinfo.gov/app/details/BILLS-119hr2821ih. 119th Congress, H.R. 2821, Introduced in House 10 Apr. 2025.
Bluebook
H.R.2821 - 119th Congress (2025-2026): FDA Modernization Act 3.0, H.R.2821, 119th Cong. (2025), https://www.govinfo.gov/app/details/BILLS-119hr2821ih.
