The Committee for Human Medicines (CHMP) of the European Medicines Agency (EMA) has granted conditional marketing authorization for the Pfizer and BioNTech vaccine against COVID-19.

This was announced this Monday at a press conference by the executive director of the EMA, Emer Cooke, after the committee meeting that took place this Monday to evaluate the vaccine.

Following the green light from the European regulatory agency, the European Commission expects to conclude the formal approval process tomorrow, a community spokesperson informed Europa Press, despite the fact that it is a bureaucracy that usually takes 67 days.

Thus, if no setback occurs, European countries, including Spain, will begin to receive the doses on Saturday 26, to start vaccination campaigns on Sunday 27.

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