UK Releases Draft Post Market Surveillance Requirements for Medical Devices

The UK has released a draft of its proposed Post Market Surveillance Requirements for Medical Devices. If the draft regulations, “The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2023,” are approved, they will pertain to devices sold in England, Wales, Scotland and Northern Ireland, beginning in 2024.

The draft regulations serve as an amendment to the existing UK MDR regulation and focus on Part 4A of UK MDR, post market surveillance (PMS) requirements. They include significantly more detail on the requirements for:

In addition, the draft regulations detail the process of initial reporting, investigation and final reporting of serious incidents. The draft regulations were presented to the World Trade Organisation (WTO) and are currently open to comments from WTO members.

 

 

 

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