MHRA is an executive agency, sponsored by the Department of Health and Social Care.

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...

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 …

Dec 3, 2025 · A system allowing drugs to be approved in the UK by other “trusted” regulators such as the US Food and Drug Administration (FDA) is sparking concern among experts. They say the …

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

In the past year, the European Medicines Agency (EMA), the Food and Drug Administration (FDA) and the Medicines and Healthcare Products Regulatory Agency (MHRA) authorised 53 novel drugs.

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

1 day ago · Learn what to expect during an MHRA inspection, the most common findings, and how to prepare with a practical step-by-step guide.

Jan 29, 2024 · “Today’s announcement by the MHRA expands treatment options to even more patients suffering from life-threatening invasive candidiasis infections globally,” said Taylor Sandison, M.D. …

Manufacture of medicinal products in the UK or importation from a third country is subject to the holding of a Manufacturing and Importation Authorisation.