Webinar
Medical Devices

AIMDD to MDR Transition - What You Need to Know

The webinar provides an overview of important topics to be considered when transitioning from the AIMDD to the Medical Device Regulation (MDR).

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In this webinar:

Pre-Submission preparations & considerations.
MDR Technical documentation review process.
General feedback on technical documentation.
Post application activities & responsibilities.

Speakers

Hear from the experts in this webinar

Speaker

Thomas Doerge

Global Head Active Implantable Medical Devices, BSI

Speaker

Concetta Gallo

Technical Team Manager, AIMD, BSI

Informatie en media

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