Catalogue description Medicines and Healthcare Products Regulatory Agency (MHRA): Committee Files

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Details of MHRA 12
Reference: MHRA 12
Title: Medicines and Healthcare Products Regulatory Agency (MHRA): Committee Files
Description:

This series contains files relating to expert committees or sub-committees and board papers from the Medicines and Healthcare Products Regulatory Agency (MHRA) including: Commission on Human Medicine (CHM), The Medicines Commission, Committee on Safety of Medicine, Committee on Safety of Drugs (Sub-Committee on Chemistry, Pharmacy and standards), the Committee on Dental and Surgical Materials, Pharmacovigilance Expert Advisory Group (PEAG, Sub-Committee of CHM), Biologicals/Vaccines Expert Advisory Group (BVEAG, Sub-Committee of CHM), Committee on Review of Medicines (and Immunologicals Sub-Committee) and the Committee on Safety of Drugs
Date: 1970-2002
Related material:

MH 55
Held by: The National Archives, Kew
Legal status: Public Record(s)
Language: English
Creator:

Department of Health, 1988-

Department of Health and Social Security, 1968-1988
Physical description: 3 file(s)
Access conditions: Open unless otherwise stated
Immediate source of acquisition:

From 2020 Medicines and Healthcare Products Regulatory Agency
Accruals: Series is accruing.
Administrative / biographical background:

The Medicines and Healthcare Products Regulatory Agency (MHRA) was created in 2003. It assumed the responsibilities of the Medicines Control Agency (MCA), created in 1989, and the Medical Devices Agency (MDA), created in 1993. Prior to the creation of the MCA and MDA, the regulation of medicines and medical devices was undertaken by policy divisions in the Department of Health and Social Care (DHSC). When the Agency was created the records collection was split between MHRA and DHSC. The files in this series represent those for which MHRA retained ownership.

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