H.R.2821

FDA Modernization Act 3.0

Chamber Passed·7/21/26

FDA Modernization Act 3.0 requires the FDA to update regulations to replace animal testing references with nonclinical testing references.

FDA Modernization Act 3.0 mandates the Secretary of Health and Human Services, through the Commissioner of Food and Drugs, to publish a final rule updating nonclinical testing methods. The rule will amend sections of title 21, Code of Federal Regulations, to replace references to animal tests with nonclinical tests. It also adds the definition of "nonclinical test" to specified sections. The interim final rule will become effective immediately without requiring the Secretary to demonstrate good cause.

Included in complete analysis

  • Overview
  • Core Provisions
  • Implementation
  • Impact
  • Legal Framework
  • Critical Issues

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Where it stands

Last
Passed the House · Jul 21
Current
The Senate
Next
Senate floor vote

Sponsors

Democratic CaucusRepublican Caucus

History

Jul 21

Senate

Received in the Senate.

Jul 20

House

Mr. Guthrie moved to suspend the rules and pass the bill.

Jul 20

House

Considered under suspension of the rules. (consideration: CR H4639-4640)