Understanding Post Brexit Scenario for Medical Devices and Appointing a UKRP The Need of An Exclusive Webinar
It is well known that from January 1, 2021, medical devices to be placed on the UK market are obliged to follow a new Regulatory regime. Currently, the UK market is a witness to many Regulatory changes, with the impact of Brexit. The UK’s existing Regulatory Authority, the Medicines and Healthcare Products Regulatory Agency (MHRA), has taken over the European Union (EU) responsibilities, ultimately changing the UK regulations.