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Presentation at the Personal Connected Health Alliance about regulatory trends in EU regulation of software as medical device in Vienna, May 2017 Trends in EU regulation of software as medical devicePresentation at the Personal Connected Health Alliance about regulatory trends in EU regulation of software as medical device source: https://www.linkedin.com/groups/2070960/2070960-6301418599525478400 Marked as spam
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Ivan Liljegren
We're currently deep diving into the new classification rules, and are struggling with the new rule 11 route for decision support, where some software could end up in class III. Does anyone have an example of the kind of software that is targeted by this new rule? I.e. products which will now end up in class III?
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