A guide to MDR conformity assessment procedures
The first step in the process is for manufacturers to classify their medical device based on the requirements in the Medical Device Regulation (MDR).
Medical Device Regulation (MDR) guide
Are you prepared for the changes? This MDR guide will give you an overview of the key areas of focus and changes within the regulation.
How to classify your medical device
A classification guide for manufacturers getting their medical devices into the European market.