What is this webinar about?

The webinar covers the interplay between AI and the Medical Device Regulation and AI assessments of Medical Device Software during the transition period of the AI Act and after its full implementation. We will also provide guidance on how to submit a well-structured and complete technical documentation for AI expert reviews under the MDR.

What will participants gain?

We will share the essential aspects of the AI Act and the conformity assessment for Medical Device Software containing AI.

Who should attend?

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

Speakers

Thomas
Doerge
Global Head, Active Implantable Medical Devices and SaMD
 
Inma
Pérez Ruiz
AI Regulatory Lead

 

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

Email: medicaldevicesmarketing@bsigroup.com

Phone: +44 3450809000

 

 

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