National Commission is seeking evidence to shape regulation of AI in healthcare and support the UK’s ambition for a world-leading, AI-enabled NHS. Updated MHRA guidance will help health...

We publish the most up-to-date information for a medicine according to its licence history. You can use the A-Z list to find an active substance, or search for a medicine. We publish scientific...

MHRA-GMDP contains information relating to manufacturing and wholesale distribution authorisations, API registrations and GMP/GDP certificates. Notified E-cigarette products published for supply...

The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that …

We are the regulator of medicines, medical devices and blood components for transfusion in the UK. We put patients first in everything we do, right across the lifecycle of the products we regulate.

Feb 18, 2025 · The Medicines and Healthcare Products Regulatory Agency (MHRA) has published new guidance providing clarification for registration and managing registered devices in the MHRA Device …

Dec 18, 2020 · News stories and articles referencing UK Medicines and Healthcare products Agency (MHRA) on European Pharmaceutical Review

We deliver this through three distinct yet complementary business centres: the MHRA regulatory centre, the National Institute for Biological Standards and Control (NIBSC) and the Clinical...

Jan 28, 2015 · The Medicines and Healthcare Products Regulatory Agency (MHRA) website is now on GOV.UK.

Manufacturers, importers and distributors of active substances are required to register their activities with the MHRA. Since inspections of manufacturers of active substances are based on risk,...