MDR Navigator

Your trusted guide to MDR and IVDR compliance

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Medical Device Expert on MDR 2017/745, IVDR 2017/746 and related MDCG guidance

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check regulatory compliance classify medical devices prepare technical documentation manage clinical trials obtain regulatory approval

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What are the key requirements of MDR 2017/745?
How do I classify my medical device under MDR?
What is the role of the notified body in MDR?
What are the latest updates from MDCG on MDR implementation?
How can I ensure my medical device is compliant with MDR?

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