An Act 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
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Chicago
U.S. Congress. Senate. FDA Modernization Act 3.0. S. 355. 119th
Cong., 1st
sess., Engrossed in Senate December 17, 2025. https://www.govinfo.gov/app/details/BILLS-119s355es.
APA
Congress, Senate (2025, December 17). FDA Modernization Act 3.0 (S. 355 (ES)). Retrieved from https://www.govinfo.gov/app/details/BILLS-119s355es.
MLA
United States, Congress, Senate. FDA Modernization Act 3.0. U.S. Government Publishing Office, https://www.govinfo.gov/app/details/BILLS-119s355es. 119th Congress, S. 355, Engrossed in Senate 17 Dec. 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-119s355es.
