A UK Government report finds that unsafe and non-compliant products can cost businesses up to £400 per item, with hidden impacts like recalls, lost sales, and reputational damage, making compliance a key business priority.
UK consults on making CE marking recognition permanent for medical devices
The MHRA has launched a 2026 consultation on the future of CE marking in Great Britain, proposing its indefinite recognition for medical devices. The outcome could significantly impact regulatory requirements.
Trade deal between United Kingdom and India to boost economy
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.
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.
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.
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.