WEBINAR | Pre-clinical Testing Requirements under Regulation (EU) 2017/745 on Medical Devices: A Notified Body’s Perspective

Webinar recording

Webinar recording

This webinar offered a thorough understanding of the preclinical testing requirements outlined in Regulation (EU) 2017/745 on medical devices. In collaboration with TUV SUD, a leading notified body, participants gained direct access to expert knowledge essential for regulatory compliance. 

If you require any further information, contact us at: [email protected] 

 

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