WHY MATERIOVIGILANCE IS NOT PHARMACOVIGILANCE?Key Differences Explained
WHY MATERIOVIGILANCE IS NOT PHARMACOVIGILANCE? Key Differences Explained
13
Jan 26
Post-Market Surveillance and Vigilance for Medical Devices
Post-market surveillance is a critical regulatory requirement for medical devices, ensuring continuous monitoring of device performance and patient safety after market placement.
22
Jun 25
Building a Compliant Medical Device Quality Management System
A robust Quality Management System (QMS) is the foundation of medical device compliance. With increasing regulatory scrutiny, manufacturers must ensure their systems are not only compliant but inspection-ready at all times.