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

• General introduction
• Audit preparation 
• Application 
• QMS on site audit 
• Technical documentation assessment
• NC
• Q&A

Target Audience

This webinar is intended for medical device manufacturers

Language: English 

 

For further information please contact: marketing.cbe@sgs.com

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