Search For "authorization"
India's first mRNA vaccine by Gennova gets DCGI approval, to be rolled out
Updated : 3 years, 8 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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FDA denies authorization to market JUUL e-cigarettes over safety concerns
Updated : 3 years, 8 months ago IST
Maryland [US], June 24 (ANI): Citing safety concerns, the US Food and Drug Administration (FDA) issued marketing denial orders (MDOs) to JUUL Labs Inc. for their e-cigarettes among others which are currently marketed in the United States.
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PM Modi to inaugurate IN-SPACe HQ, medical college, water project in Gujar
Updated : 3 years, 9 months ago IST
Ahmedabad (Gujarat) [India], June 9 (ANI): To promote privatisation in the space sector, Indian National Space Promotion and Authorization Centre (IN-SPACe) headquarters have been set up at Bopal in Ahmedabad which will be inaugurated by Prime Minister Narendra Modi Friday.
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Bharat Biotech asked to provide more data on COVID-19 vaccine Covaxin for
Updated : 3 years, 10 months ago IST
New Delhi [India], April 22 (ANI): The Subject Expert Committee (SEC) of the Drug Controller General of India (DCGI) has asked Bharat Biotech for additional data on its COVID-19 vaccine, Covaxin, for administering it to children aged between 2-12 years, sources said.
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Novovax' COVID-19 vaccine gets emergency use authorisation for adolescents
Updated : 3 years, 11 months 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 : 3 years, 12 months 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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US revokes authorization of Chinese telecom firm over national security co
Updated : 3 years, 12 months ago IST
Washington [US], March 18 (ANI): A US communication regulator has voted to revoke the authorization of Chinese firm Pacific Networks Corp. and its wholly-owned subsidiary, ComNet (USA) LLC, to provide domestic interstate and international telecommunications services within the United States.
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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 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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228 geographical areas got nod for city gas projects till 10th bidding rou
Updated : 4 years, 1 month ago IST
New Delhi [India], February 3 (ANI): The Petroleum and Natural Gas Regulatory Board (PNGRB) responsible for granting authorization for developing of City Gas Distribution network, has up to the 10th CGD bidding round, authorized a total of 228 geographical areas (GAs), comprising 407 distric
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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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