![]() The agency also reiterated that it had not received any application for authorization of Covishield, the version of AstraZeneca's vaccine made by India's Serum Institute, adding that it could approve or accept for use only those shots with ongoing applications.įriction emerged between India and Europe in recent days over the exclusion of Covishield by the European Union vaccine passport programme as one of its accepted vaccines. ![]() The EMA said it would proceed with evaluating data from CureVac's (5CV.DE) coronavirus vaccine after the German biotech firm said late on Wednesday its jab was only 48% effective in a final analysis. The EU's drug regulator, the European Medicines Agency (EMA), said on Thursday that it had given the green light to two vaccines that target the omicron variant of COVID-19. This Q&A provides information on the following: The vaccines approved by the European Medicines Agency (EMA) as of February 2022 Vaccines under review by the. Sometimes, after the EMA or MHRA has licensed a vaccine, circumstances change such as an outbreak of a disease which necessitates the vaccine being used in a different population. According to the Czech Ministry of Health, from 23 August onward the Czech Republic will also accept Covid-19 vaccinations administered to people from. To monitor potential new threats, vaccine makers have exposed the blood of vaccinated people to viruses engineered to have the typical features of the variant of concern to determine if neutralising antibodies quell that virus.Ĭurrently, the European Union has four COVID-19 vaccines authorized: those from Pfizer (PFE.N) and BioNTech (22UAy.DE), AstraZeneca (MRNA.O) and Johnson & Johnson (JNJ.N). Vials and syringes are seen in front of displayed EU flag in this illustration photo taken March 16, 2021. BioNTech and Pfizer have started a rolling submission of their COVID-19 vaccine BNT162b2 to the European Medicines Agency (EMA).
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