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The MHRA continues to issue new guidance for medical device to support Brexit, which goes into effect on January 1.

One details how to register medical devices for use in the UK. All manufacturers must register with the MHRA before making a device available for sale in Great Britain. Anyone outside of the UK needs to appoint what is called a “Responsible Person” who is registered in the country, who will then register the device.

There are different registration deadline dates, which depend on the class of medical device.

They also issued guidance on supplying investigational medicinal products from Great Britain to Northern Ireland. Manufacturers can apply EU rules on importation requirements until Dec. 31, 2021.