UK: Regulating medical devices from 1 January 2021
From 1 January 2021 the Medicines and Healthcare products Regulatory Agency (MHRA) will take on the responsibilities for the UK medical devices market that are currently undertaken through the EU system. This guidance provides information on how the UK system will operate, including for:
• Getting your device certified
• Conformity marking your device
• Registering your device with the MHRA.