Jan 10, 2024
What is the EU Person Responsible for Regulatory Compliance (PRRC) role in the EU MDR?
Jan 10, 2024
European Medical Device Importers and Distributors Have New Regulatory Responsibilities Under EU MDR Articles 13 and 14
Jan 10, 2024
Table of Contents for the EU MDR 2017/745
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?
