How to Succeed at Your First MDR Audit

This webinar will help you prepare for your first Medical Devices Regulation audit.

The Medical Devices Directive is now void and Medical Devices Regulation (MDR) 2017/745 is now applicable for all medical devices sold in Europe. SGS was recently designated an MDR Notified Body, and we will soon begin auditing against MDR requirements. We have set up this webinar to help you succeed at your first MDR audit.

For further information, please contact:

Victoria Leo
Marketing Specialist
t: +1 201 508 3000