Government to align with European specifications on high risk in vitro diagnostic devices to reduce regulatory burden 

New government funding will help make the boldest ideas in UK life sciences a reality.

MHRA seeks views on possible amendments to the Medical Devices Regulations 2002 to include common specification requirements for manufacturers of IVD devices.

List of Field Safety Notices from 10 to 14 November 2025.

Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.

Zydus Pharmaceuticals UK LTD has informed the MHRA that there is an error on the artwork for the outer carton and Patient Information Leaflet (PIL) of Topiramate Zydus Pharmaceuticals UK 20mg/ml Oral Solution (pack size 150ml and 280ml bottles).

As with all licensed medicines, we will continue to monitor its safety closely as it becomes more widely used