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.
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).
How to classify your medical device
A classification guide for manufacturers getting their medical devices into the European market.
Medical training guide - Spring 2019
This training guide provides an overview of our public training portfolio for all medical device regulation and ISO 13485 courses, which focus on training that is relevant to your industry & business.