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S. 355

FDA Modernization Act 3.0

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, and may make other changes to the regulations as appropriate. 

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

Held at the desk.

Sen. Booker, Cory A. [D-NJ](D-NJ)Sponsor
9 cosponsors4 D4 R1 I
9cosponsors1committees10actions1amendments1related bills5subjects
  1. FloorH15000

    Held at the desk.

  2. FloorH14000

    Received in the House.

  3. Floor

    Message on Senate action sent to the House.

  4. Floor

    Passed Senate with an amendment by Unanimous Consent. (text of amendment in the nature of a substitute: CR S8794)

  5. Floor17000

    Passed/agreed to in Senate: Passed Senate with an amendment by Unanimous Consent.

  6. Floor

    Measure laid before Senate by unanimous consent. (consideration: CR S8793-8794)

  7. Discharge

    Senate Committee on Health, Education, Labor, and Pensions discharged by Unanimous Consent.

    Health, Education, Labor, and Pensions Committee
  8. Committee14500

    Senate Committee on Health, Education, Labor, and Pensions discharged by Unanimous Consent.

    Health, Education, Labor, and Pensions Committee
  9. IntroReferral

    Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

    Health, Education, Labor, and Pensions Committee
  10. IntroReferral10000

    Introduced in Senate