Select Page
nonconforming materials report

MDR 2017/745 Questions Answered

This White Paper covers frequently asked questions about the new EU MDR 2017/745. It covers questions around applicability, auditing, notified bodies, Common Specifications, Regulatory Compliance Officer, Medical Device Coordination Group, Technical Documentation, and reporting. 


Additional MDR 2017/745 White Papers:

Changing Regulatory Expectations: Events that Shaped the New EU Medical Device Regulation and Changed Expectations

Get your FREE White Paper here!

* These fields are required.