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House passes bill directing FDA to update animal testing rules

Published

22 July 2026

Topic

opportunities

Sectors

Digital Health

Geography

United States

Source

Read at fiercebiotech.com

Verified

Fusion42 · 22 July 2026 · Fusion42 review

The U.S. House passed the FDA Modernization Act 3.0, directing the FDA to update regulations to permit alternatives to animal testing in drug development, aligning federal rules with a 2022 law that already allowed non-animal methods. The bill awaits Senate approval and would accelerate the shift toward new approach methodologies (NAMs) such as organoids and organs-on-chips, with the FDA aiming to make animal studies the exception rather than the norm within three to five years.

This Wire brief sits within Fusion42's coverage of Digital Health. Wire is Fusion42's founder-focused intelligence feed: each story is connected to the funds and startups it names — every one with a live profile on Raise or Scout — so founders can follow the capital and the momentum behind the headline rather than just the headline itself. Wire analysis is one of the live surfaces Arthur reasons over.

The Wire takeaway

If you make organs-on-chips, organoids, or any lab model that predicts human biology, you now have legal cover to replace animal testing in FDA submissions—and the regulator will look at your data even if it's not yet formally qualified. The money spent on animal testing by every pharma company just became available for you to capture.

Related on Wire

Topics

Digital Health · fda-regulation · preclinical-testing · nams-organoids · drug-development · compliance-cost