H.R. 2821House Bill119th Congress

FDA Modernization Act 3.0

Passed 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, 2025Last action Jul 21, 2026
Introduced in HouseApr 10, 2025
Reported by CommitteeMay 21, 2026
Passed HouseJul 20, 2026
Senate considerationNow

Being considered by the Senate

Become Law

This house bill has been approved by the House of Representatives and is now before the Senate.

Who introduced this

Earl Carter

Earl Carter

R

U.S. Representative · GA-1

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