2019/01/08 - Regulatory Affairs - Cord Schloetelburg
EU MDR Factsheet for Manufacturers of Medical Devices
Medical device manufacturers must implement the new EU MDR. Here you will find an overview to get things going.
transition period
2019/01/03 - Regulatory Affairs - Cord Schloetelburg
Medical Device Certification Based on the New EU MDR: a Step by Step Guide
Medical device certification is a prerequisite for market access in Europe. Use this checklist to start certification based on the new EU MDR.