Decentralised manufacture: UK Guideline on Good Manufacturing Practice (GMP)

How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.

List of Field Safety Notices from 18 to 22 August 2025.

Viatris has received reports of brown discolouration and blockage in the needle of pre-filled syringes of Arixtra. This quality defect is related to oxidation of the syringe needle.

Operation Pangea brings together health regulators, customs authorities, law enforcement agencies, and private sector partners to tackle the threat posed by global criminal networks

The Medicines and Healthcare products Regulatory Agency (MHRA) has approved Siiltibcy

You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.