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...

The MHRA products website allows you to find: The leaflets which are provided with medicines; The description of the medicinal product’s properties and how it can be used; Scientific reports...

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...

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 …

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 …

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

2025年2月12日 · GB-only Licensing Process: Even if Marketing Authorisation Holders (MAHs) wish to market their products only in Great Britain, they are no longer be able to apply for a GB …

Beginning January 1, 2025, medicines for supply in the UK are now authorized UK-wide by the Medicines and Healthcare products Regulatory Agency (MHRA) only and therefore, …

2014年5月28日 · Queries on registering and submitting product licence applications using the MHRA Portal, phone: 020 3080 7100 or email [email protected]. MHRA …

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 …