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Medicines and Healthcare products Regulatory Agency
Additional recommended knowledge
The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK government agency which is responsible for ensuring that medicines and medical devices work and are acceptably safe.
The agency was formed on 1 April 2003 with the merger of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA). It is an Executive Agency of the Department of Health.
Roles of the MHRA
MHRA hosts and supports a number of expert advisory bodies, including the Commission on Human Medicine which replaced the Committee on the Safety of Medicines in 2005, and the British Pharmacopoeia Commission.
As part of the European system of approval, MHRA or other 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 other members as and where requested.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Medicines_and_Healthcare_products_Regulatory_Agency". A list of authors is available in Wikipedia.|