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...

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...

2014年12月18日 · How to package medicines for sale and what information you must provide to consumers and healthcare professionals. The MHRA approves all packaging and labelling …

The MHRA public access registration database (PARD) website allows you to find: Registered manufacturers. Registered medical device types

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 …

2023年8月8日 · Manufacturers placing products on the Great Britain market (England, Scotland, and Wales) must register their product with the Medicines and Healthcare products Regulatory …

–The MHRA will provide a scientific opinion on new medicines that will treat, diagnose or prevent life threatening, or seriously debilitating conditions without adequate treatment options before …

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 …

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

Regarding the Manufacturing Plant under (1) the Active Substance(s) Exported to the EU for Medicinal Products for Human Use are identified in Annex 1.