Eine Spritze mit der Aufschrift "Covid-19" liegt auf einem aufgeschlagenen Impfausweis.
(Symbolfoto: Milton Oswald - stock.adobe)
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EU-Prüfung
Die Europäische Arzneimittelbehörde (EMA) mit Sitz in Amsterdam gibt eine Empfehlung für die Zulassung des Impfstoffes in der Europäischen Union. Die endgültige Entscheidung fällt auf dieser Basis die EU-Kommission, die in der Regel dem EMA-Votum folgt.
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