Town Hall – FDA’s Quality Management System Regulation (QMSR): Medical Device Risk-Based Inspections

Town Hall – FDA’s Quality Management System Regulation (QMSR): Medical Device Risk-Based Inspections The U.S. Food and Drug Administration (FDA) will host a town hall for industry and other interested parties to discuss the updated Inspection of Medical Device Manufacturers Compliance Program (CP) Manual (CP 7382.850), effective February 2, 2026. This CP includes the new inspection process, which aligns with…