20:13 GMT28 February 2021
Listen Live
    World
    Get short URL
    9521
    Subscribe

    BRUSSELS (Sputnik) - The European Medicines Agency (EMA) told Sputnik that it completed scientific consultations with Russia's Gamaleya research centre that developed the Sputnik V coronavirus vaccine, which means that Moscow can now submit an application for vaccine authorization for the EU market.

    "The Gamaleya National Centre of Epidemiology and Microbiology has received scientific advice from EMA for the development of its Sputnik V vaccine (formerly known as Gam-COVID-Vac) for the prevention of COVID-19 ... As a next step the application for a marketing authorisation could then be prepared by the company," a EMA spokesperson said.

    The scientific consultations are a well-established process, available for all companies and meant to facilitate their development programs, a EMA spokesperson explained.

    "EMA will provide advice to companies taking into account the latest regulatory and scientific guidance," the agency assured.

    The EU drug regulator has not yet received a marketing authorization request from the Sputnik V developers.

    "We cannot point to an agreed timetable at the moment. As soon as we receive an application from the company, we will communicate about this," the spokesperson noted.

    The Russian Direct Investment Fund (RDIF) told Sputnik on Tuesday that it had an official confirmation that the European Medicines Agency (EMA) accepted all paperwork for registration of Russia's Sputnik V vaccine in the EU market.

    RDIF, Sputnik V vaccine developers and the EMA held a scientific consultation on the vaccine on 19 January, the fund recalled.

    "On 29 January 2021, the RDIF submitted an application for Sputnik V vaccine registration in the European Union, it started presenting information to the EMA through the rolling review procedure. The fund has an official confirmation from the EMA that the application was accepted. The speed of application approval is determined by the EMA," the RDIF said.

    If a conditional marketing authorization is issued and the vaccine is approved by the European Commission, it will be possible to deliver Sputnik V to the EU through centrally-managed procedures. The bloc made decisions on centralized vaccines procurement even before the first vaccines were approved. The EU signed contracts with six coronavirus vaccine manufacturers. Thanks to these contracts, the EU countries will have access to over 2.3 billion doses of vaccines. The EU expects around 70 percent of European citizens to be vaccinated by the end of summer.

    However, in recent weeks, the EU faced shipment delays and reductions in the number of doses that were initially agreed upon with AstraZeneca and Pfizer.

    Sputnik V, developed by the Gamaleya Epidemiology and Microbiology Centre, was the world's first vaccine against COVID-19 and was registered by the Russian health ministry on 11 August.

    Tags:
    consultations, Russia, European Union, Sputnik V
    Community standardsDiscussion