Search For "emergency use authorization"
Vaccine regulators, officials meet to strategize integration of COVID-19 v
Updated : 2 years, 4 months ago IST
To integrate pandemic vaccines in national immunisation programme in countries of the WHO South-East Asia Region, vaccine regulators, and officials from WHO today began deliberating strategies to enable member countries to transition from the use of COVID-19 vaccines under Emergency Use Auth
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DCGI's subject expert committee to hold discussion on 'Five Arms' intranas
Updated : 3 years, 4 months ago IST
DCGI has already given emergency use authorization (EUA) to BBIL for the intranasal vaccine. BBIL had in September this year applied for DCGI's approval for market authorization of its "Five Arms" intranasal heterologous booster dose, and it has now announced that iNCOVACC (BBV154) has re
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Bharat Biotech-made iNCOVACC becomes world's first intranasal COVID vaccin
Updated : 3 years, 6 months ago IST
New Delhi [India], September 6 (ANI): The Drugs Controller General of India (DCGI) rendered an emergency use authorization (EUA) to Bharat Biotech for the intranasal vaccine- iNCOVACC, said officials on Tuesday.
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India's first mRNA vaccine by Gennova gets DCGI approval, to be rolled out
Updated : 3 years, 9 months ago IST
Pune (Maharashtra) [India], June 29 (ANI): India's first indigenously developed mRNA vaccine against the COVID-19 gets the Emergency Use Authorization (EUA), to be sold under the brand name GEMCOVAC™-19 and will be rolled out soon, informed the officials on Wednesday.
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Novovax' COVID-19 vaccine gets emergency use authorisation for adolescents
Updated : 4 years ago IST
New Delhi [India], March 23 (ANI): Novavax on Tuesday announced the first emergency use authorization of its COVID-19 vaccine for adolescents falling in the age bracket of 12-18 years in India.
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Moderna requests FDA to authorize second COVID-19 booster shot for adults
Updated : 4 years ago IST
Washington [US], March 18 (ANI/Xinhua): American biotechnology company Moderna submitted a request to the U.S. Food and Drug Administration (FDA) on Thursday for emergency use authorization (EUA) on a fourth dose of its COVID-19 vaccine for adults 18 years of age and older, who already recei
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Decision on mixing, matching of COVID-19 vaccine booster dose will be base
Updated : 4 years ago IST
New Delhi [India], March 3 (ANI): The Union Health Ministry on Thursday said that any decision on the mixing and matching of the booster dose of COVID-19 vaccines will be taken based on science.
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SEC recommends COVID-19 vaccine Corbevax for 12-18 year age group: Sources
Updated : 4 years, 1 month ago IST
New Delhi [India], February 15 (ANI): The Drugs Controller General of India (DCGI)'s Subject Expert Committee (SEC) has recommended Emergency Use Authorization to Hyderabad-based pharmaceutical company Biological E's COVID-19 vaccine, Corbevax, for the age group 12 to 18 years subject to
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Pfizer, BioNTech seek emergency authorization for COVID-19 vaccine for kid
Updated : 4 years, 1 month ago IST
New York [US], February 2 (ANI): The pharmaceutical companies, Pfizer and BioNTech, are seeking Emergency Use Authorization for their COVID-19 vaccine for use in children between six months and four years of age.
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Moderna's 'Spikevax' COVID19 vaccine gets full approval by FDA
Updated : 4 years, 1 month ago IST
Washington [US], February 1 (ANI): Moderna's COVID-19 vaccine 'Spikevax' received full approval from the U.S. Food and Drug Administration (FDA), after more than a year of its "emergency use authorization", reported USA TODAY.
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Novavax, Serum Institute file for emergency use authorisation of Novavax'
Updated : 4 years, 2 months ago IST
Gaithersburg [US], January 10 (ANI): Novavax, a biotechnology company dedicated to developing and commercializing next-generation vaccines for serious infectious diseases, and Serum Institute of India (SII), on Monday, announced a regulatory submission to the South African Health Products Re
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Affordable, effective COVID-19 vaccine Corbevax to be especially useful in
Updated : 4 years, 2 months ago IST
Houston [US], December 29 (ANI): Texas Children's Hospital and Baylor College of Medicine announced on Tuesday (local time) that Corbevax, a protein sub-unit COVID-19 vaccine, whose technology was created and engineered at its Center for Vaccine Development (CVD), has received Emergency Use
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