Jul 20, 2021
Non-Product Software (NPS) Validation for Medical Device Manufacturers
Jun 02, 2021
You’ve Evaluated Every Risk But Are You Properly Documenting Medical Device Benefits?
Apr 23, 2021
FDA 21 CFR Part 11 Compliance: Are You Complying With These Four Critical Electronic Records Requirements?
Apr 01, 2021
Latest EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) Updates
Mar 29, 2021
MDSAP Mock Audits – Getting QA and RA on the Same Page
Feb 24, 2021
Virtual Medical Device Inspections and Audits: Here to Stay?
