The Medicines and Healthcare products Regulatory Agency (abbreviated MHRA) is a statutory body in the United Kingdom that seeks to find and eliminate harm in a medicinal product or medical device at any stage of its development or use thereby permitting graded (i.e. either the product is licensed to be a prescription only medicine authorised by a pharmacist [P, or a General Sales List (GSL) product) legality of that product, or a licence. MHRA is an executive agency of the Department of Health.
The roles of the MHRA are:
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 rappoteur or co-rappoteur 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.
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