Nov 02, 2023
Definitive Guide to Medical Device Clinical Evaluation Reports (CER) and EU MDR Requirements
Sep 30, 2023
EU MDR Equivalence: How Equivalent Does a Medical Device Need to Be According to MEDDEV 2.7/1 rev 4?
Feb 14, 2023
What Is Considered a Significant Change Under EU MDR Article 120(3) and MDCG 2020-3?
Feb 13, 2023
An Overview of Medical Device Periodic Safety Update Reports (PSUR) and Postmarket Surveillance Reports (PMSR) Under the EU MDR
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
