MHRA - MHRA guidance on new Medical Devices Post-Market Surveillance requirements

15th January 2025

MHRA - MHRA guidance on new Medical Devices Post-Market Surveillance requirements

A suite of guidance has been published by the Medicines and Healthcare products Regulatory Agency (MHRA). This guidance is designed to help medical device manufacturers understand and prepare for the new Post-market surveillance (PMS) regulation for medical devices in Great Britain (GB) which will come into force on the 16th June 2025.

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