Nov 27 (Reuters) – French drugmaker Valneva said on Monday that the application for its vaccine candidate against mosquito-borne viral disease chikungunya was accepted by the European Medicines Agency (EMA) which would now examine the drug in a fast-track procedure.
The EMA “has determined that all essential regulatory elements required for scientific assessment were included in the application,” Valneva said in a statement.
Accelerated assessment reduces the timeframe the EMA review to 150 days from 210 days, Valneva said.
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Morning Briefing
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EU lawmakers have approved new rules aimed at strengthening how failing banks are managed, extending protections to a wider range of institutions and depositors across the bloc.
The p...
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