Here’s how the UK will regulate medical devices after Brexit

Spread the love

Image from Jonathan Chng/Unsplash

The United Kingdom issued an outline of how it intends to regulate medical devices beginning in 2021 after Brexit.

From Jan. 1, 2021, the responsibilities for the UK medical devices market that are currently governed by the European Union (EU) will be taken over by the Medicines and Healthcare products Regulatory Agency (MHRA), the guidance said.

Get the full story on our sister site, Medical Design & Outsourcing.

Comments are closed, but trackbacks and pingbacks are open.