Search results
Results from the WOW.Com Content Network
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.
The Commission on Human Medicines (CHM) is a committee of the UK's Medicines and Healthcare products Regulatory Agency. It was formed in October 2005, and assumed the responsibilities of the Medicines Commission and the Committee on Safety of Medicines. Membership in this various and extensive body is listed on a governmental website.
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 ...
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 ...
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.
The Human Medicines Regulations 2012 in the United Kingdom were created, under statutory authority of the European Communities Act 1972 and the Medicines Act 1968 in 2012. . The body responsible for their upkeep is the Medicines and Healthcare products Regulatory Age
Medicines for Human Use in the United Kingdom are regulated by the Medicines and Healthcare products Regulatory Agency (MHRA). The availability of drugs is regulated by classification by the MHRA as part of marketing authorisation of a product. [citation needed] The United Kingdom has a three-tiered classification system: [citation needed]