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Prior to the UK's departure from the European Union in January 2021, the MHRA was part of the European system of approval. Under this system, national bodies can be the rapporteur or co-rapporteur for any given pharmaceutical application, taking on the bulk of the verification work on behalf of all members, while the documents are still sent to ...
After an early change of name to MHRA in 1918, the unincorporated charity became an incorporated company with the same name on 2 October 1997. Its declared aim is to encourage and promote advanced study and research in the field of the modern humanities , which include the modern and medieval European languages, literatures and cultures.
Modern Humanities Research Association, UK MHRA Style Guide, an academic style guide; Other uses. Men's human rights activism This page was last edited on 13 ...
It is run by the Medicines and Healthcare products Regulatory Agency (MHRA) and the Commission on Human Medicines. It was extended to hospital pharmacists in 1997, and to community pharmacists in 1999. [2] The Yellow Card Centre Scotland is a joint venture between MHRA and the Scottish Government. [3]
The MHRA Style Guide: A Handbook for Authors, Editors, and Writers of Theses—formerly the MHRA Style Book—is an academic style guide published by the Modern Humanities Research Association. It is most widely used in the arts and humanities in the United Kingdom , where the MHRA is based.
Dame June Munro Raine DBE (née Harris; born 1952), is a British doctor who is currently serving as the Chief Executive Officer of the Medicines and Healthcare products Regulatory Agency (MHRA) in the United Kingdom. [1] Raine spent much of her career in the Medicines Division of the MHRA (and in its predecessor, in the Department of Health ...
Anthony Harnden MB FRCGP is the Chair of the Medicines and Healthcare products Regulatory Agency (MHRA). He is a professor of primary care at the University of Oxford and until December 2024 was a registrant council member of the General Medical Council (GMC) and Chair of the Remuneration Committee.
Marketing Authorisation Application (MAA) is an application submitted by a drug manufacturer seeking marketing authorisation, that is permission to bring a medicinal product (for example, a new medicine or generic medicine) to the market.