This presentation is aimed at helping developers navigate the development and regulation maze of MDR for medical device software. Some key points like safety and performance aspects for medical device software, Clinical Validation for Medical Device Software and Regulatory Referential for Medical Device Software – Europe and more are discussed.
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presentation by
Christophe Amiel, M.Sc.
Senior Director, Medical Devices & Digital Life Sciences
As a Senior Director at VCLS, Christophe is responsible for leading the Medical Device and Digital Life Science Group. The…
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