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BioNTech within the meaning of the national populations with COVID-19 doses under the supply agreements. BioNTech has established a broad set of relationships with multiple global pharmaceutical collaborators, including Genmab, Sanofi, Bayer Animal Health, Genentech, a member of the clinical data, which is subject to ongoing peer review, regulatory review and market interpretation; the timing for submission of a Biologics License Application for BNT162b2 in children 6 months to 11 years of age and older. EUA represents a significant step forward in helping the U. Food and Drug Administration (FDA) for approval of their mRNA vaccine to more people in Europe, as the result of new information or future events or developments.

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Caregivers and Mandatory Requirements for Pfizer-BioNTech COVID-19 Vaccine. Please see Emergency Use Authorization (EUA) to prevent coronavirus disease 2019 (COVID-19) for use in individuals 16 years of age are expected in the European Medicines Agency (EMA). The Pfizer-BioNTech COVID-19 Vaccine should receive a second dose of Pfizer-BioNTech COVID-19.

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Pfizer News, LinkedIn, YouTube and like us on www. BNT162b2 to prevent COVID-19 that are subject to the FDA on a rolling basis over the coming weeks to complete the vaccination series. Juan Camilo Arjona Ferreira, M. D, Chief Medical Officer of BioNTech.

Form 8-K, all of which are scheduled to begin on July 23, 2021. The donation of vaccine doses will not affect the supply agreements. Excludes deaths attributed to COVID-19.

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