The European Commission has published today 9 Factsheets related to the MDR and IVDR.
The documents present main changes, new requirements, transition timeline and frequent Questions & Answers in a comprehensive manner. They are particularly relevant for:
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Manufacturers of medical devices and IVDs;
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Authorised Representatives, Distributors, Importers;
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Authorities in non-EU/EEA States;
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Persons responsible for procurement of medical device within hospitals, clinics,etc.
You can consult newly published Factsheets here as well as all the rest of Useful documents in our MDlaw library.
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