Consumer Safety Officer, Special Assistant, Office of Medical Device and Radiological Health Inspectorate (OMDRHI), Medical Products Inspectorate (MPI), Office of Inspections and Investigations (OII) FDA (Invited)
Are you ready? You are required to be in compliance with the QMSR as of February 2, 2026! Immediately following the QMSR Implementation Update session, FDA will discuss updates to the Compliance Program (CP) for Inspection of Medical Device Manufacturers that both reflects the new QMSR regulations and incorporates content for PMA Pre/Post Approval Inspections.
Don’t miss this detailed follow-on session. If you anticipate FDA interaction, you will want to understand this update!
