HR. 340In Committee
The HCT/P Modernization Act of 2025
Plain-English overview
What this bill does
Require the FDA to educate stakeholders and report to Congress on regulating human cell and tissue products, including Tissue Reference Group guidance and manufacturer oversight data
Key points
- Establish public comment docket
- Require FDA workshops
- Require congressional recommendations report
- Require annual HCT P oversight data
Current status
Where it stands
Status
In Committee
Latest action
2025-01-13 — 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.