What is the webinar about?

The webinar covers the Medical Device Regulation requirements for Software including GSPRs, Applicable guidance, lessons learnt and the interplay between AI and the MDR. 

Who should attend?

Start-ups, SMEs, Software developers, Medical device software companies

What will participants gain?

We will share the important aspects of the Technical Documentation and typical gaps we see as a notified body for software applications applying for MDR certification.

Speakers

Thomas
Doerge
Global Head AIMD and SaMD
 
 

To find out more about Medical Devices visit our dedicated Medical Devices webpage and follow us on LinkedIn at BSI Medical Devices.

Email: medicaldevices@bsigroup.com

Phone: +44 3450809000

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