FDA Modernization Act 3.0
Sponsor

Full profile: /officials/B001288
Source: Congress.gov · FEC
Cosponsors (9)
Members who have signed on to support this bill since introduction. Source: Congress.gov.
- Angus S. King Jr. (I-ME)Original· 2025-02-03
- Ben Ray Luján (D-NM)Original· 2025-02-03
- Eric Schmitt (R-MO)Original· 2025-02-03
- John Kennedy (R-LA)Original· 2025-02-03
- Rand Paul (R-KY)Original· 2025-02-03
- Richard Blumenthal (D-CT)Original· 2025-02-03
- Roger Marshall (R-KS)Original· 2025-02-03
- Sheldon Whitehouse (D-RI)Original· 2025-02-03
- Adam B. Schiff (D-CA)· 2025-07-22
Latest Action
The most recent step in the bill's legislative path. Committee Activity below shows referrals and reports; the full action-by-action history including floor proceedings lives at Congress.gov →
Committee Activity
Currently in
- Senate Committee on Health, Education, Labor, and PensionsDischarged From · 2025-12-17
Previously
- Senate Committee on Health, Education, Labor, and PensionsReferred To · 2025-02-03
Plain-English Summary
FDA Modernization Act 3.0 This bill requires the Food and Drug Administration (FDA) to publish an interim final rule implementing a provision of the Consolidated Appropriations Act of 2023 that authorized the use of certain alternatives to animal testing to support investigational use of a new drug. The rule must replace references to animal tests, data, studies, models, and research with references to nonclinical tests, data, studies, models, and research throughout the FDA’s regulations governing investigational new drug applications, and may make other changes to the regulations as appropriate. The rule must be published within one year of the bill’s enactment, and must take immediate effect as an interim final rule.
Plain-English rewrite of the Congressional Research Service summary published on Congress.gov. Cached and reviewed.
Subjects
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