Search Results - Medicines and Healthcare products Regulatory Agency
Medicines and Healthcare products Regulatory Agency
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 Agency (MCA) and the Medical Devices Agency (MDA). In April 2013, it merged with the National Institute for Biological Standards and Control (NIBSC) and was rebranded, with the MHRA identity being used solely for the regulatory centre within the group. The agency employs more than 1,200 people in London, York and South Mimms, Hertfordshire. Provided by Wikipedia
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Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2017
Published 2017“…Great Britain Medicines and Healthcare products Regulatory Agency…”
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Rules and guidance for pharmaceutical manufacturers and distributors 2015
Published 2015“…Medicines and Healthcare products Regulatory Agency…”
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Rules and guidance for pharmaceutical distributors 2015
Published 2015“…Medicines and Healthcare products Regulatory Agency…”
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Rules and Guidance for Pharmaceutical Distributors 2017
Published 2017“…Great Britain Medicines and Healthcare products Regulatory Agency Inspection, Enforcement, and Standards Division…”
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