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H.R. 2821

BillFederalHousePassed House
FDA Modernization Act 3.0
About This Bill
Passed
Latest Action · April 10, 2025
Referred to the House Committee on Energy and Commerce.
Congress
119th (2025–2027)
Introduced
April 10, 2025
Cosponsors (41)
21D 20R
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Summary

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

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