TThe EPSCO council decided in December 2022 to recommend extensions of the MDR transition timelines until 2028 for Class III and IIb devices and until 2027 for lower class of devices. Join our webinar, where our experts will cover what the impact can be for the manufacturer and what will be the most relevant way to continue moving forward. 

Objective

The objective of this webinar is to present the last update on MDR, following the decision to extend MDR transition timelines, as well as the best approach for manufacturers to move forward towards MDR. 

 

Agenda

• Introduction
• What do we know about MDR extension?
• Impact on manufacturer 
• Submitting your application 
• What your certification process will be like 
• Q&A

Target Audience: This webinar is aimed at medical devices manufacturer quality or regulatory affairs managers.

Language: English
Cost: No Charge

Can't make a live session? Register now and receive a complimentary recording after the live event. For further information, please contact: KNGlobalMarketing@sgs.com

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