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Overview Our 2025/26 business plan gives a continued commitment to…
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.
Information on Medicines and Healthcare products Regulatory Agency spending over £25,000.
MHRA transactions over £500 made using the government procurement card (GPC).
A programme to help decision making across the lifecycle of products, benefitting both regulatory and health technology assessment (HTA) evaluations.
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.
Meeting minutes taken from meetings of the Vaccine Benefit Risk Expert Working Group (VBREWG) held between 10 May 2021 to 25 May 2021.
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