FOI release

Freedom of Information request on animal trials (FOI 21-396)

Published 28 June 2021

1st May 2021 FOI 21/396

Dear

Thank you for your email of 11th April where you have asked: “I would like full information about these animal trials, for the following reasons: 1) If the animal tests are worth doing, why do you not give information about them? 2) I feel that the least we can do for those sacrificed for our wants is to acknowledge the debt. 3) I need to weigh up the pros and cons of accepting the vaccine(s). Ingredients are published so it looks like they are suitable for vegans in that respect, but animal tests are also relevant to a vegan. May I ask you to provide information on the animal tests that the vaccines have undergone? Also, can you justify requiring tests on species other than the intended species, a) ethically b) scientifically c) regarding efficiency, seeing as the animal tests will have to be ignored for the purpose of doing them all again (suitably modified) on humans?”

Information on the animal trials conducted can be found within the Public Assessment Reports for each vaccine which are available on the MHRA website. Links to these are provided below: https://www.gov.uk/government/publications/regulatory-approval-of-pfizer-biontech-vaccine-for-covid-19
https://www.gov.uk/government/publications/regulatory-approval-of-covid-19-vaccine-astrazeneca https://www.gov.uk/government/publications/regulatory-approval-of-covid-19-vaccine-moderna

Regarding the question concerning animal testing in general, by law new medicines are required to be tested on animals before they can advance to phase testing on human volunteers in clinical trials.

If you have a query about the information provided, please reply to this email

If you are dissatisfied with the handling of your request, you have the right to ask for an internal review. Internal review requests should be submitted within two months of the date you receive this response and addressed to: [email protected]

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Please remember to quote the reference number above in any future communications.

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 at:

Information Commissioner’s Office Wycliffe House Water Lane Wilmslow Cheshire SK9 5AF

Yours sincerely

MHRA Customer Service Centre

Medicines and Healthcare products Regulatory Agency 10 South Colonnade, Canary Wharf, London E14 4PU