H.R. 2821119th CongressHouse Bill

FDA Modernization Act 3.0

Introduced in the House

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. The rule must be published within one year of the bill’s enactment, and must take immediate effect as an interim final rule.

Introduced Apr 10, 2025
Introduced in HouseApr 10, 2025
Reported by CommitteeMay 21, 2026
3
House vote

Awaiting a vote in the House

4
Become Law

This house bill has been filed and is working its way through Congress. It will need to pass both the House and the Senate, then be signed by the President to become law.

Who introduced this

Earl Carter

Earl Carter

Republican

U.S. Representative · GA-1

Bipartisan — 41 cosponsors (21 D, 20 R)

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