The UK and India have signed a landmark 2025 Free Trade Agreement, cutting tariffs on 90% of goods to boost exports, trade, and long-term economic growth.
Use of CE marking on construction products beyond June 2025
Last year, the UK Government has confirmed an extension to the recognition of the CE marking for construction products beyond the previously planned deadline of June 2025. This decision has allowed manufacturers to continue placing const
UK PMS Regulations applicable from June 2025
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.
Great Britain’s June cosmetics deadlines: new restrictions on Kojic Acid and BHT
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.
New Post-Market Surveillance Requirements Applicable from June 2025
UK post-market surveillance rules for medical devices change in June 2025. Learn what manufacturers must do to stay compliant.
Great Britain April deadline for cosmetic products
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.
MHRA Updates UK Medical Device & IVD Registration Guidance
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.
UK Upcoming February 2025 cosmetics deadlines: BHT restrictions
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.
Latest developments on the future of the UK Medical Devices Regulations
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.
Key insights for placing your medical device on the UK 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.