Freedom of Information request on clinical data received for the authorised vaccines (FOI 21-803)
Published 27 April 2022
3rd August 2021 FOI 21/803
Dear
Thank you for your email.
Please note that clinical data is routinely published by the EMA on their website, including clinical data received for the authorised vaccines. A link to these is provided below: https://clinicaldata.ema.europa.eu/web/cdp
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/
If you have a query about the information provided, please reply to this email
Please remember to quote the reference number above in any future communications.
Yours sincerely
MHRA Customer Service Centre
Medicines and Healthcare products Regulatory Agency 10 South Colonnade, Canary Wharf, London E14 4PU