Und Nummer drei ist im Anmarsch: AstraZeneca hat Antrag endlich auf Zulassung für die EU gestellt.
ergänzend dazu, Freigabe frühestens 29.1
ZitatAn opinion on the marketing authorisation could be issued by 29 January during the meeting of EMA’s scientific committee for human medicines (CHMP), provided that the data submitted on the quality, safety and efficacy of the vaccine are sufficiently robust and complete and that any additional information required to complete the assessment is promptly submitted.