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A programme to help decision making across the lifecycle of products, benefitting both regulatory and health technology assessment (HTA) evaluations.
1. Overview The MHRA data strategy sets out an ambition to promote…
Performance data for MHRA key performance indicators (KPIs) and information on the expected timeline to complete a specific regulatory function.
Overview Our 2025/26 business plan reaffirms MHRA’s commitment to…
This privacy notice describes how we collect and use your personal information, in accordance with the Data Protection Act and the General Data Protection Regulation.
At the Medicines and Healthcare products Regulatory Agency (the Agency) we…
Information on Medicines and Healthcare products Regulatory Agency spending over £25,000.
MHRA transactions over £500 made using the government procurement card (GPC).
Annual Report of the Human Medicines Regulations 2012 Advisory Bodies - the Commission on Human Medicines (CHM) and the British Pharmacopoeia Commission.
MHRA annual report and accounts 2024 to 2025.
Information about how we handle potential corporate conflicts of interest (COI) between different parts of the Agency.
These reports outline the MHRA’s Corporate and Business Plans, detailing the agency's strategic direction over the next three years.
MHRA performance metrics for clinical trials and established medicines assessment.
Progress made in delivering the Patient Involvement Strategy, October 2021 - January 2025.
Meeting minutes taken from meetings of the Vaccine Benefit Risk Expert Working Group (VBREWG) held between 20 September 2022 and 5 May 2023.
Meeting minutes taken from meetings of the Vaccine Benefit Risk Expert Working Group (VBREWG) held between 1 June 2021 and 19 November 2021.
Meeting minutes taken from meetings of the Vaccine Benefit Risk Expert Working Group (VBREWG) held between 3 December 2021 and 29 March 2022.
Meeting minutes taken from meetings of the Vaccine Benefit Risk Expert Working Group (VBREWG) held between 13 April 2022 and 25 August 2022.
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