UK MEDICAL DEVICE REGULATION : GUIDANCE AND TRANSITIONAL TIMELINES
Great Britain, 25 February 2026 – The landscape of UK medical device regulation has undergone significant transformation following the UK’s departure from the European Union. Navigating the requirements for Great Britain (GB), Northern Ireland (NI), and the European Union (EU) is essential for manufacturers to ensure uninterrupted market access. The Medicines and Healthcare products Regulatory […]
UK MEDICAL DEVICE REGISTRATION: MHRA GUIDANCE SETS PATH FOR 2026 TRANSITION
United Kingdom, 25 February 2026 — The UK medical device registration landscape is the MHRA guidance updated in February 2026: “Register medical devices to place on the market.” The document outlines a significant shift in how devices are registered, paid for, and maintained in Great Britain and Northern Ireland. Specifically, the MHRA is moving away […]