In a UK-first, the Medicines and Healthcare products Regulatory Agency (MHRA) and Barts Health NHS Trust have developed a DNA sequencing approach that can be implemented...

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...

British Pharmacopoeia: The BP makes an important contribution to the role of the Medicines and Healthcare products Regulatory Agency (MHRA) in protecting public health by...

2014年5月28日 · How to contact the MHRA for specific services or enquiries. Review the information below and choose the most relevant contact for your enquiry. Selecting the …

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 medicines and medical devices work and are acceptably safe.

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

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,...

Due to the restrictions caused by COVID-19, the period of validity GMP and GDP certificates issued by MHRA is automatically extended until the end of 2024, except where clarifying remarks in the...

2025年2月12日 · MHRA: For products with parallel import permission (both UK and EU markets) or medicines named for patient use or nationally authorised medicines in UK by EMA before 2021, MHRA had readable access as products were authorised and available in Northern Ireland only. This is recorded in Article 57 also called as EudraVigilance Database [20].

2020年12月31日 · What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets. The Medicines and Healthcare products Regulatory Agency (MHRA) is responsible...