European Commission publishes NEW Information sheets

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:

  • Manufacturers of medical devices and IVDs;

  • Authorised Representatives, Distributors, Importers;

  • Authorities in non-EU/EEA States;

  • 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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