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The agency said its experts will “evaluate data as they become available to decide if the benefits outweigh the risks” of the vaccine. The rolling review will continue until “enough evidence is available for a formal marketing authorization application,” the EMA said, adding that it could not predict timelines. The announcement from the Amsterdam-based agency came a day after a top World Health Organization official said the WHO is set to decide this week whether to approve two Chinese COVID-19 vaccines for emergency use. !! EMA human medicines committee (#CHMP) has started a rolling review of #COVID19vaccine (Vero Cell) Inactivated, developed by Sinovac Life Sciences Co., Ltd.

Noord hollandMariangela simaoEu medicines agencyEuropean unionEuropean medicines agencyWorld health organizationSinovac life sciences co ltdAmerican developed novavaxVero cellநூற்த் ஹாலண்ட்ஐரோப்பிய தொழிற்சங்கம்உலகம் ஆரோக்கியம் ஆர்கநைஸேஶந்வெரோ செல்