WEBINAR | How to best interact with a Notified Body for a successful MDR Application

Webinar recording

Webinar recording

This webinar explores the intricate processes involved in the qualification and classification of medical devices (MDs) under the Regulation (EU) 2017/745 or MDR.

Asphalion expert Koldo Garcia and BSI expert Pilar Maldonado provide a detailed overview of the conformity routes available under MDR, providing guidance through the compliance landscape to ensure MDs meet the stringent European legislation.

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