Feb 13, 2023
An Overview of Medical Device Periodic Safety Update Reports (PSUR) and Postmarket Surveillance Reports (PMSR) Under the EU MDR
Jan 29, 2023
Dig Deep and Do Medical Device Root Cause Analysis the Right Way
Jan 04, 2023
EU MDR Timeline: Common Questions Answered About the Implementation Extension
Jan 02, 2023
EU MDR Vigilance Reporting Requirements and MEDDEV 2.12-1 Rev 8
Dec 17, 2022
Creating a Problem-Solving Culture in Your Organization
Nov 22, 2022
What Is a Medical Device Software Bill of Materials (SBOM)?
