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.
On April 13, 2022, the United Kingdom notified the draft “The Toys and Cosmetic Products…
Manufacturers of medical devices, IVDS, and cosmetics, are you aware of the new UK requirements…
Regardless the outcome of the ongoing EU trade negotiations, Brexit will imply certain consequences for…
The Spanish Agency of Medicines and Medical Devices (AEMPS) has published a Checklist to verify…
Preparing for different Brexit scenarios, the UK government published a guidance covering the EU Exit…
On the 18th of July, the European Commission published a Notice to stakeholders regarding the…