Brief

The MHRA invites sponsors and researchers to discuss COVID-19 vaccine regulatory strategies and filing plans in the UK. To support development, the agency provides expert advice on rolling reviews, risk management planning, and Good Manufacturing Practice. Applications are prioritized for thorough assessment of safety, quality, and efficacy. Companies are also encouraged to discuss batch release testing approaches with the MHRA's Innovation Office by submitting an enquiry form or emailing innovationoffice@mhra.gov.uk.

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Medicines and Healthcare products Regulatory Agency (MHRA)

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