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H.R. 1532 119th Congress House

Scientific EXPERT Act of 2025

Official title: To amend the Federal Food, Drug, and Cosmetic Act to establish a process for externally led, science-focused drug development meetings, and for other purposes.

Introduced: February 24, 2025 Introduced by: Doris O. Matsui Democratic · California See on congress.gov
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 Everywhere this bill has been 2 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Feb 24, 2025
Referred to the House Committee on Energy and Commerce.
Feb 24, 2025
Introduced in House
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What's happening now February 24, 2025

Referred to the House Committee on Energy and Commerce.

 Plain-English summary Congressional Research Service

Scientific External Process for Educated Review of Therapeutics Act of 2025 or the Scientific EXPERT Act of 2025

This bill requires the Food and Drug Administration (FDA) to facilitate and participate in externally led, science-focused drug development meetings to discuss the development of treatments for rare diseases and conditions. 

The FDA must enter into an arrangement with the Reagan-Udall Foundation for the FDA under which the foundation agrees to convene such meetings. Meetings must be held at least four times a year, and each meeting must focus on a different rare disease or condition. 

The foundation must establish a permanent steering committee to review and recommend topics for each meeting. In evaluating potential topics, the committee must consider unmet therapeutic needs, patient population sizes for different diseases and conditions, and whether a disease or condition would benefit from clarity and alignment on drug development questions, among other factors. 

In planning each meeting, the foundation must develop a list of medical experts, drug sponsors, scientific organizations, patient organizations, and other entities to be invited to participate. Representatives of the FDA’s review divisions must attend each meeting. 

After each meeting, the foundation must make available a summary of the meeting noting areas of consensus, areas where additional clarification or information is needed, and next steps agreed upon with the FDA.

The bill also requires the FDA to indicate whether it incorporated any input from these meetings when approving a new drug or biologic. 

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 Bill text 1 version

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APA
U.S. Congress. (2026). H.R. 1532: Scientific EXPERT Act of 2025. 119th Congress. Open America. https://openamerica.io/bill/119-HR-1532/
MLA
"H.R. 1532: Scientific EXPERT Act of 2025." 119th Congress, 2026, Open America, https://openamerica.io/bill/119-HR-1532/.
Bluebook (legal)
H.R. 1532, 119th Cong. (2026), https://openamerica.io/bill/119-HR-1532/.
Markdown link
[H.R. 1532: Scientific EXPERT Act of 2025](https://openamerica.io/bill/119-HR-1532/)
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