September 10, 2020
Regulating Medical Devices After Brexit
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. The agency has published a guidance on what you need to know to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets from 1 January 2021.
The complete guidance can be accessed through the Medicines and Healthcare products Regulatory Agency (MHRA).