Search results
Results From The WOW.Com Content Network
Website. www.gov.uk /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 ensuring that medicines and medical devices work and are acceptably safe. The MHRA was formed in 2003 with the merger of the Medicines Control ...
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. Initially, the Book and Guide were only available ...
Modern Humanities Research Association. The Modern Humanities Research Association (MHRA) is a United Kingdom–based international organisation that aims to encourage and promote advanced study and research of humanities. It is most notable for producing the MHRA Style Guide.
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]
www.nibsc.org. The National Institute for Biological Standards and Control (NIBSC) is a government agency that works in the field of biological standardisation and is part of the United Kingdom's Medicines and Healthcare products Regulatory Agency (MHRA). It is responsible for developing and producing over 90% of the biological international ...
On 2 December 2020, the UK became the first country to give approval for use of the Pfizer–BioNTech vaccine, [36] [37] later branded as Comirnaty. [38] This was in the form of a temporary authorisation given by the Medicines and Healthcare products Regulatory Agency (MHRA) under Regulation 174 of the Human Medicines Regulations 2012. [39]
Commission on Human Medicines. 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 ...
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. MAA is part of the official procedure before the Medicines and Healthcare products Regulatory Agency in the ...