Hong Kong — BioNTech and Moderna could receive conditional EU marketing authorisation for their Covid-19 vaccines in the second half of December, according to the head of the EU’s executive arm, putting the bloc on track to start distributing the shots at the same time as the US.

The European Medicines Agency (EMA) is in daily contact with the US Food and Drug Administration (FDA) about the evaluation of the vaccines to “synchronise” assessment, said European Commission president Ursula von der Leyen. The EMA has said conditional approval could come as early as the second half of December, Von der Leyen told reporters after EU leaders discussed the Covid-19 pandemic via video conference on Thursday...

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