H.R.2821

FDA Modernization Act 3.0

Chamber Passed·7/21/26

Prefiled

Introduced

Chamber Passed7/21/26

Final Passage

Complete

Engrossed

H. R. 2821

April 10, 2025

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

A BILL

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.

Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,

SECTION 1. Short title.

This Act may be cited as the “FDA Modernization Act 3.0”.

HR2821 U.S. House: FDA Modernization Act 3.0