Jan 11, 2024
Medical Device Registration under UK MHRA: UKCA Marking Requirements, UK Responsible Person, and More
Jan 11, 2024
Understanding EU MDR Clinical Evidence Required for Legacy Medical Devices as Outlined in MDCG 2020-6
Jan 11, 2024
6 Things R&D Engineers Need to Know About the EU Medical Device Regulation
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
