Regulating medical devices in the UK
Regulating medical devices in the UK What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets. From: MHRA) is responsible for regulating the UK medical devices market. This guidance provides information on the UK system, including for: getting your device certified MHRA This guidance is divided into sections on the different rules that apply in Great Britain, Northern Ireland and the EU. Great Britain is England, Wales and Scotland. For Northern Ireland, different rules apply to those in Great Britain. For more information on th...
Source: gov.uk