HR. 340In Committee
The HCT/P Modernization Act of 2025
Requires the FDA to share information, gather input, and report to Congress on regulating human cell and tissue products
Plain-English overview
What this bill does
Requires the FDA to share information, gather input, and report to Congress on regulating human cell and tissue products
Key points
- Establish public comment docket
- Require FDA workshops
- Require Congress report
- Require HCT P website disclosures
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
undefinedAdministrative law and regulatory proceduresCell biology and embryologyCongressional oversightDepartment of Health and Human ServicesGovernment information and archivesHealthHealth information and medical records