What does Preamble of FDA Modernization Act 3.0 do?

This bill requires 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.

What does SHORT TITLE. of FDA Modernization Act 3.0 do?

This bill is formally titled the FDA Modernization Act 3.0.

What does REGULATIONS ON NONCLINICAL TESTING METHODS. of FDA Modernization Act 3.0 do?

This section directs the Secretary of Health and Human Services to publish an interim final rule within one year of the Act's enactment. The rule aims to amend sections of the Code of Federal Regulations to replace references to 'animal' tests with 'nonclinical' tests. It also mandates adding the definition of 'nonclinical test' to specific sections of the Code of Federal Regulations. The interim final rule will become immediately effective without requiring a demonstration of good cause. Section 505 of the Federal Food, Drug, and Cosmetic Act is amended to redesignate a subsection as 'aa'.

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FDA Modernization Act 3.0

Last updated: 4/10/2025 · Introduced: 4/10/2025

Author: Earl Carter (R-GA)

TL;DR (AI)

The bill requires the Food and Drug Administration to update regulations by replacing references to 'animal' tests with 'nonclinical' tests.
It mandates the addition of a 'nonclinical test' definition to relevant sections of the Code of Federal Regulations.
The FDA must publish an interim final rule within one year of enactment, which will take immediate effect.

119th Congressin committeeOfficial page

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Other Sections

Includes provisions on preamble, short title., and 1 more.

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