Join our webinar, in which we will present the latest update on MDR, following the decision to extend MDR transition timelines, as well as the best approach for manufacturers to move forward towards MDR.
In December 2022, the EPSCO council decided to extend the MDR transition timeline to 2027 for Class III and IIb devices and to 2028 for lower classes of devices. Join our webinar, where our experts will cover the potential impact on manufacturers and the most relevant ways to continue moving forward.
Agenda
- Introduction
- What do we know about the MDR extension?
- Impact on manufacturers
- Submitting your application
- What your certification process will be like
- Q&A
Target Audience: This webinar is aimed at medical device manufacturers and quality and regulatory affairs managers.
Language: English
Cost: No charge
Register Now
There will be two sessions of this webinar:
For further information, please contact us.