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Influenza: Vaccination

Asked by Esther McVeyConservativeDepartment of Health and Social CareTabled Answered 12 May 2025UIN 50102

The question

To ask the Secretary of State for Health and Social Care, with reference to FOI2025/00320, for what reason the Adjuvanted Zoonotic Influenza Vaccine was authorised via UK Regulation 56.

Answered by Karin Smyth

Adjuvanted Zoonotic Influenza Vaccine (Surface Antigen, Inactivated) Seqirus suspension for injection in a pre‐filled syringe (PLGB 47991/0013) was authorised by the Medicines and Healthcare products Regulatory Agency via UK Regulation 56 of The Human Medicines Regulations 2012 on 6 October 2023. This created a duplicate unbranded licence that was identical to Aflunov suspension for injection in a pre-filled syringe (PLGB 47991/0004), which was authorised in the United Kingdom on 29 November 2010 by a European Commission decision, following a centralised procedure by the European Medicines Agency (EMA; EMEA/H/C/002094). Subsequent to the granting of this duplicate unbranded licence, further lifecycle management actions were authorised for this licence.

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