MHRA issue new guidance for registering all medical devices in the UK


The MHRA have published new guidance for companies that place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets from 1 January 2021. Registration of all devices will be required on the MHRA DORS system, which mandates using the GMDN as the device nomenclature. More information can be found at https://www.gov.uk/guidance/regulating-medical-devices-from-1-january-2021#registrations-in-great-britain