Jan 11, 2024
Future Proofing Your Medical Device QMS for Global UDI Expansion
Jan 11, 2024
ISO/TR 20416: Best Practices for Medical Device Postmarket Surveillance
Jan 11, 2024
Regulatory Implications of “Reshoring” or Relocating Your Medical Device Manufacturing Facility
Jan 11, 2024
Medical Device Incident and Adverse Event Reporting Timelines in 6 Major Markets
Feb 13, 2023
An Overview of Medical Device Periodic Safety Update Reports (PSUR) and Postmarket Surveillance Reports (PMSR) Under the EU MDR
Feb 24, 2021
Virtual Medical Device Inspections and Audits: Here to Stay?
