From 16 June 2025, the Medical Devices Post-market Surveillance (PMS) Regulations apply to medical devices and IVDs placed on the market in Great Britain. Published in 2024, the new UK PMS Regulations amends the UK Medical Devices Regulations (MDR) 2002.
The UK cosmetics industry is facing two key regulatory deadlines this June, as new restrictions on Kojic Acid and Butylated Hydroxytoluene (BHT) come into effect under the UK Cosmetics Regulation.
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.
