Freedom of Information request on real time safety surveillance of all COVID-19 vaccines currently used in the UK (FOI 21-751)
Published 27 April 2022
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5th August 2021 FOI 21/751 Dear
Thank you for your email.
The MHRA is conducting almost real time safety surveillance of all COVID-19 vaccines currently used in the UK. Many people across the whole Agency contribute to the work on licensing and monitoring the safety of COVID vaccines so it is not possible to give an exact number. In the Division responsible for vigilance and risk management for medicines, there are a total of 137 FTEs. The division’s responsibilities include receiving Yellow Card reports and monitoring the benefits and risks of COVID-19 Vaccines in use.
If you disagree with how we have interpreted the Freedom of Information Act 2000 with regards to your request, you can ask for the decision to be reviewed. The review will be carried out by a senior member of the Agency who was not involved with the original decision. Internal review requests should be submitted within two months of the date you receive this response and addressed to: [email protected]
If you were to remain dissatisfied with the outcome of the internal review, you would have the right to apply directly to the Information Commissioner for a decision. Please bear in mind that the Information Commissioner will not normally review our handling of your request unless you have first contacted us to conduct an internal review. The Information Commissioner can be contacted online: https://ico.org.uk/make-a-complaint/official-information-concerns-report/official-information-concern/
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Yours sincerely
MHRA Customer Service Centre
Medicines and Healthcare products Regulatory Agency 10 South Colonnade, Canary Wharf, London E14 4PU