MHRA Guidance: Regulating Medical Devices in the UK
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The Medicines and Healthcare products Regulatory Agency (MHRA) is responsible for regulating the UK medical devices market.
This guidance from the MHRA details what you need to do to place a medical device on the Great Britain, Northern Ireland, and European Union (EU) markets.
Specifically, this guidance provides information on:
- Getting your device certified
- Conformity marking your device
- Registering your device with the MHRA
Added on: 04 October 2024