MD3/IVD3: The impact of MDR/IVDR and its effect on future developments of policies, manufacturers and inspectorates

By Maïté Barthel2024-11-08T06:56:00

Key points:

Collaboration builds expertise: collaboration among all players would clear doubts and build knowledge to streamline compliance with the Medical Devices Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR)
Proactivity and communication: Medtech should consult at an earlier stage with Notified bodies to ensure successful submission

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