Freedom of Information request (FOI 22/934)
Published 17 January 2024
FOI 22/934
26th September 2022
Dear
Thank you for your email.
A full list of ingredients for each of the vaccines is available in the SmPCs that are published by MHRA on our website (https://products.mhra.gov.uk/). Before a product is authorised for use in the UK, testing from suitably qualified and inspected laboratories is provided to show that it complies with specific release and shelf-life specifications that prove it is of a high enough standard to be used in patients.
All batches of licenced Covid vaccines that have been used in the UK vaccination programme have been independently tested under Statutory Rules for testing.
The testing carried out for different vaccines is based on the EU Guidelines for Official Control Authority Batch Release (OCABR) for Human Biologicals: Vaccines, blood and plasma derivatives which can be found on the European Directorate for the Quality of Medicines and Healthcare (EDQM) website. Human OCABR Guidelines - European Directorate for the Quality of Medicines & HealthCare (edqm.eu). Within this link the requirements for testing of influenza vaccines is outlined.
Covid vaccines are tested according to the OCABR activities related to COVID-19 vaccines - European Directorate for the Quality of Medicines & HealthCare (edqm.eu).
If you have a query about the information provided, please reply to this email.
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Cheshire
SK9 5AF
Yours sincerely
MHRA Customer Experience Centre