HR. 1532In Committee
Scientific EXPERT Act of 2025
Plain-English overview
What this bill does
Requires the FDA to take part in externally led scientific meetings on rare disease drug development and use a structured process to gather and report input from those meetings
Key points
- Establish foundation steering committee
- Require FDA participation in meetings
- Require input disclosure in approvals
- Direct meeting summaries and next steps
Current status
Where it stands
Status
In Committee
Latest action
2025-02-24 — Referred to the House Committee on Energy and Commerce.
Related context
Topics and policy areas
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Discovery signals
About these signals
Impact and Momentum are relative discovery aids calculated by Legislation Lemur. They help you scan the congressional record; they are not predictions, endorsements, ideological ratings, or measures of policy importance.
Impact ScoreOverall observed legislative footprint and accumulated activity.
MomentumHow recently active or changing the bill appears in available data.