Medical Device and IVD Registration in the UK

The regulatory landscape for medical devices and IVDs in the United Kingdom (U.K.) and European Union (EU) has transformed post-Brexit, requiring manufacturers and distributors to adopt new compliance strategies for trade.

Our expert, Karen Hill of Emergo by UL, breaks down the essential steps manufacturers and distributors need to take to meet region-specific requirements. Learn about the latest registration requirements, CE and UKCA markings and the special conditions under the Northern Ireland protocol. Staying ahead of these critical changes will help organizations successfully navigate the UK and EU’s complex evolving regulatory frameworks and maintain cross-border market access.