Discover key insights for placing medical devices on the UK market post-Brexit. Learn about UKCA and CE marking options, appointing a UK Responsible Person, MHRA registration, and regulatory compliance to access the Great Britain market.

Discover key insights for placing medical devices on the UK market post-Brexit. Learn about UKCA and CE marking options, appointing a UK Responsible Person, MHRA registration, and regulatory compliance to access the Great Britain market.
Millions of tonnes of plastic waste is produced and imported into the UK every year…
A standard can be understood as a harmonised way of doing something. It usually contains…
On April 13, 2022, the United Kingdom notified the draft “The Toys and Cosmetic Products…
On October 27, 2021, The U.S. Food and Drug Administration (FDA), Health Canada, and the…