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Bill · HR

H.R. 1532 (119th)

Scientific EXPERT Act of 2025

Original

referredUnited States· United States Congress· EN

Introduced

24 February 2025

Last action

24 February 2025 · Introduced

Status

Referred to the House Committee on Energy and Commerce.

Sponsors

Doris Matsui, Rep. Bilirakis, Gus M. [R-FL-12], Paul Tonko, Lloyd Doggett, Del. Norton, Eleanor Holmes [D-DC-At Large], Rep. Fitzpatrick, Brian K. [R-PA-1]

Subjects

Healthcare

Source updated

21 August 2026

Healthcare

Summary

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. 

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 24 February 2025

    Introduced

    Referred to the House Committee on Energy and Commerce.

    Source: IntroReferral

  2. 24 February 2025

    Introduced

    Introduced in House

    Source: IntroReferral

  3. 24 February 2025

    Introduced

    Introduced in House

    Source: IntroReferral

Votes

No vote records are attached yet.

Versions

No version snapshots stored. Document URLs remain at the source.

Documents

2 official files

Sponsors

Related records

Sources

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Scientific EXPERT Act of 2025 — United States — PoliticalRepo