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What is Medicines and Healthcare products Regulatory Agency mean?
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.
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| Men's Human Rights Movement | Community |
| Michigan Hot Rod Association | Community |
| Men's Human Rights Activism | General |
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| Medicines and Healthcare products Regulatory Agency | Governmental |
| Medicines and Healthcare products Regulatory Agency (UK) | Governmental |
| Minnesota Human Rights Act | Governmental |
| Medical Hair Restoration Australia | Regional |
Posted on 25 Nov 2024, this text provides information on Miscellaneous in Governmental related to Governmental. Please note that while accuracy is prioritized, the data presented might not be entirely correct or up-to-date. This information is offered for general knowledge and informational purposes only, and should not be considered as a substitute for professional advice.
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