Guidance
The European Commission provides a range of guidance documents to assist stakeholders in implementing the medical devices regulations.
These are legally non-binding guidance documents, whose main purpose is ensuring uniformity in the application of the regulations
Click the below button to consult all guidance documents
The Medical Devices Coordination Group (MDCG) has endorsed documents on the following subjects:
- UDI
- EUDAMED
- European Medical Device Nomenclature
- Notified bodies Clinical Investigation and Evaluation
- New Technologies
- Other topics
- Other Guidance documents
Dernières mises à jour
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Publié18 Janvier 2021Sous: Medical Devices - Sector, Medical Devices - New regulations, Medical Devices - Topics of Interest
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Publié11 Janvier 2021Sous: Medical Devices - Sector, Medical Devices - New regulations, Medical Devices - Topics of Interest
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Publié01 Décembre 2020Sous: Medical Devices - Sector, Medical Devices - New regulations, Medical Devices - Topics of Interest, Medical Devices - Dialogue between interested parties, Medical Devices - Expert Panels, Medical Devices - EUDAMED
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