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Dear Sir/Madam **ASK-77118 ( https://servicedesk.ema.europa.eu/jira/browse/ASK-77118 ) - Zulassungsantrag und Beurteilungsbericht für den Impfstoff Comirnaty (ehemals BNT162b2) von Biontech / Pfizer [#208045] received on 7/Jan/21** Thank you for submitting your request. This is an automated response to confirm that we have received your request; please do not respond directly to this message as this email address is not monitored. A member of Agency staff will now review your request. We will send an acknowledgement of receipt to the email address you have provided, quoting your unique reference number. We endeavour to review all requests as soon as possible, but no later than within 48 hours of receipt, during our normal business hours (see Business hours and holidays ( https://www.ema.europa.eu/en/about-us/contact/business-hours-holidays )). Should you need to contact us in relation to this request please submit your updated query through the webform ( https://www.ema.europa.eu/en/about-us/contact/send-question-european-medicines-agency ), quoting the ASK reference number given above. Kind regards,