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Synopsis Separately, an assessment of Sputnik V by a French delegation of scientists in advance of the EMA review found that the vaccine developers were unable to document that the so-called master cell bank, the initial building block of the vaccine. Agencies The developers of Russia’s Sputnik V coronavirus vaccine have repeatedly failed to provide data that regulators deem to be standard requirements of the drug approval process, according to five people with knowledge of European efforts to assess the drug, providing new insight into the country’s struggle to win foreign acceptance of its product. Reuters reported last month that the European Medicines Agency (EMA)’s review of the drug’s safety and efficacy was delayed because a June 10 deadline to submit data on the vaccine s clinical trials was missed, according to one of those people, who is close to the agency, and another person familiar with the matter. The

United statesSlovak republicFrance generalNoord hollandCecil czerkinskyVladimir putinSergio rezendeEuropean unionEuropean medicines agencyReuters the gamaleya instituteRussia gamaleya instituteRussian direct investment fundGamaleya instituteRussian president vladimirNorth americanஒன்றுபட்டது மாநிலங்களில்