First Covid-19 vaccine for EU authorised by EMA : vimarsana.

First Covid-19 vaccine for EU authorised by EMA
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Following the EMA’s recommendation, the European Commission must also give the vaccine the green light to begin the roll-out to member states.
The European Medicines Agency (EMA) has today (21 December) recommended a conditional marketing authorisation for the Covid-19 vaccine developed by Pfizer-BioNTech.
Following a rigorous evaluation of the vaccine, named Comirnaty, the EMA’s human medicines committee has concluded that there is sufficiently robust data on the quality, safety and efficacy of the vaccine to recommend it for use.
Emer Cooke, executive director of the EMA, said today’s news is an important step forward in the fight against the pandemic. “We have achieved this milestone thanks to the dedication of scientists, doctors, developers and trial volunteers as well as many experts from all EU member states,” she said.

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