Introduction
MD Directive is now void and MD Regulation 2017/745 is now applicable for all MD sold in Europe. SGS has been designated as an MDR Notified body recently and we will soon start auditing again MDR requirements, so this webinar has been set up to help you preparing your first MDR audit.
Objectives
Be prepared for your first MDR audit
Agenda
Target Audience
This webinar is intended for medical device manufacturers
Language: English
For further information please contact: marketing.cbe@sgs.com
_1725754950210