Search For "authorization"
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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SII thanks Centre for granting emergency use nod for COVID-19 vaccine Cov
Updated : 4 years, 2 months ago IST
Pune (Maharashtra) [India], December 28 (ANI): Serum Institute of India on Tuesday expressed gratitude to the Union Health Ministry for granting Emergency Use Authorization for its COVID-19 vaccine Covovax.
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South Korea approves Pfizer's COVID-19 oral pill for emergency use
Updated : 4 years, 2 months ago IST
Seoul [South Korea], December 28 (ANI/Global Economic): 'Paxlovid,' the COVID-19 oral treatment developed by a global pharmaceutical company Pfizer, received emergency use authorization from the Ministry of Food and Drug Safety (MFDS) on the 27th. It is expected to be used from the end of Ja
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SEC recommends emergency use authorization of Covovax, Corbevax vaccines f
Updated : 4 years, 2 months ago IST
New Delhi [India], December 28 (ANI): After reviewing all applications and data, the Subject Expert Committee (SEC), a body under India's drug regulator, has recommended granting the Emergency Use Authorization (EUA) to Serum Institute of India's COVID-19 vaccine Covovax and Corbevax vacc
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US grants emergency use authorization for Merck's COVID-19 pill
Updated : 4 years, 2 months ago IST
Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Thursday said that it has granted an emergency use authorization for Merck's antiviral pill Molnupiravir that is used to treat COVID-19 patients.
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US to prohibit retiring B-1B bombers until replaced with new models
Updated : 4 years, 3 months ago IST
Washington [US], December 11 (ANI/Sputnik): The United States will prohibit its Air Force from decommissioning strategic B-1B Lancer bombers until they are replaced by B-21 Raiders, the Defense News website reported, citing the 2022 National Defense Authorization Act.
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Taiwan could join RIMPAC naval exercise following the US defence policy bi
Updated : 4 years, 3 months ago IST
Taipei [Taiwan], December 11 (ANI): Taiwan navy could join Rim of the Pacific Exercise from next year under a defense policy bill for the fiscal year 2022 passed by the U.S. House of Representatives.
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UN extends mandate for int'l forces fighting piracy off coast of Somalia
Updated : 4 years, 3 months ago IST
New York [US], December 4 (ANI/Xinhua): The United Nations (UN) Security Council on Friday renewed for an additional three months its authorization for states and regional organizations cooperating with Somalia to use all necessary means to fight piracy off the coast of the East African coun
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Covaxin for 2-18 yrs: Centre examining Expert Committee recommendations, i
Updated : 4 years, 3 months ago IST
New Delhi [India], November 30 (ANI): The Central government is examining the recommendation of the Subject Expert Committee (SEC) regarding the grant of market authorization of Covaxin for the age group of 2 to 18 years for restricted use in an emergency situation subject to various cond
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US Senator introduces measure to trigger sanctions if Russia escalates Ukr
Updated : 4 years, 3 months ago IST
Washington [US], November 20 (ANI/Sputnik): US Senate Foreign Relations Chairman Bob Menendez introduced a measure this week that would trigger a broad range of sanctions against the Russian government if it engages in or supports a significant escalation of hostilities in or against Ukra
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COVID-19: US FDA expands emergency use authorizations for Pfizer, Moderna
Updated : 4 years, 3 months ago IST
Washington [US], November 19 (ANI): The US Food and Drug Administration on Friday (local time) expanded the emergency use authorization (EUA) for the Pfizer and Moderna COVID-19 vaccine boosters signaling that the shots can be given to anyone aged 18+ at least six months after completion of
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