Page 27 - மயோ சிகிச்சையகம் தடுப்பூசி ஆராய்ச்சி குழு News Today : Breaking News, Live Updates & Top Stories | Vimarsana

Published Friday, February 26, 2021 5:09PM EST Vaccine advisers to the US Food and Drug Administration voted Friday to recommend the agency grant emergency use authorization to Johnson & Johnson s coronavirus vaccine. The FDA s Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted unanimously to recommend EUA of the vaccine in people 18 and older. Acting FDA Commissioner Dr. Janet Woodcock and Dr. Peter Marks, head of the FDA s vaccine decision, said EUA would come quickly. The U.S. Food and Drug Administration has informed the sponsor that it will rapidly work toward finalization and issuance of an emergency use authorization. The agency has also notified our federal partners involved in vaccine allocation and distribution so they can execute their plans for timely vaccine distribution, they said in a joint statement after the vote.

United statesSouth africaWhite houseDistrict of columbiaArnold montoRochelle walenskyAnthony fauciNational institute of allergyUniversity of michigan school public healthUs centers for diseaseDrug administrationMayo clinic vaccine research groupAdvisory committee on immunization practicesProducts advisory committeeRelated biological products advisory committeeGreg poland