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

Description

The FDA will host a town hall 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 the requirements of the Quality Management System Regulation (QMSR).

More »