Search For "emergency use authorisation"
SEC recommends granting emergency use authorisation to Serum Institute of
Updated : 4 years ago IST
New Delhi [India], March 4 (ANI): The Subject Expert Committee (SEC) has recommended granting emergency use authorisation (EUA) to Serum India of India's COVID-19 vaccine Covovax for the age group 12-17, said the official sources.
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DCGI gives emergency use authorisation to COVID-19 vaccine Corbevax for 12
Updated : 4 years, 1 month ago IST
New Delhi [India], February 21 (ANI): Hyderabad-based pharmaceutical company Biological E on Monday received emergency use authorisation from Drugs Controller General of India (DCGI) for its COVID-19 vaccine Corbevax for the 12 to 18 age group.
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Philippines FDA approves world's first generic version of Pfizer's anti-Co
Updated : 4 years, 2 months ago IST
Manila [Philippines], January 26 (ANI/PNN): The Philippines Food and Drug Administration (FDA) has approved the world's first generic version of Pfizer's anti-Coronavirus pill Paxlovid, just days after the original was granted Emergency Use Authorisation (EUA) by the US FDA.
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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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Covovax authorisation is a vital step in India, where additional vaccine o
Updated : 4 years, 2 months ago IST
Gaithersburg/Pune (Maryland/Maharashtra)[US/India], December 29 (ANI): Novavax, Inc. (Nasdaq: NVAX), a biotechnology company dedicated to developing and commercializing next-generation vaccines for serious infectious diseases, and Serum Institute of India (SII), the world's largest vaccin
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Dr Reddy's laboratories gets DCGI's nod to launch Molnupiravir capsules in
Updated : 4 years, 2 months ago IST
Hyderabad (Telangana) [India], December 28 (ANI): Drugs Controller General of India (DCGI) on Tuesday approved Dr Reddy's laboratories for the emergency-use authorisation) to manufacture and market the oral anti-viral drug Molnupiravir capsules 200mg for the treatment of adult patients with
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DCGI grants Cipla emergency use authorisation for COVID-19 drug Molnupirav
Updated : 4 years, 2 months ago IST
Mumbai (Maharashtra) [India], December 28 (ANI): Drug Controller General of India (DCGI) on Tuesday granted Emergency Use Authorisation (EUA) to Cipla for the launch of Molnupiravir in the country for COVID-19 treatment.
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US authorizes AstraZeneca's Evusheld for pre-exposure prevention of COVID-
Updated : 4 years, 3 months ago IST
New Delhi [India], December 9 (ANI): AstraZeneca's Evusheld (Tixagevimab co-packaged with Cilgavimab), a long-acting antibody (LAAB) combination, has received emergency use authorisation (EUA) in the US for the pre-exposure prophylaxis (prevention) of COVID-19, with first doses expected t
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Bharat Biotech's partner seeks Covaxin approval in US for children below 1
Updated : 4 years, 4 months ago IST
New Delhi [India], November 6 (ANI): Bharat Biotech's US partner Ocugen has announced that it had asked the US Food and Drug Administration (FDA) for Emergency Use Authorisation (EUA) of Covaxin for children below 18.
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G-20 leaders agreed to help optimise WHO procedures for Covid-19 vaccines
Updated : 4 years, 4 months ago IST
Rome [Italy], October 31 (ANI): Leaders of the G-20 nations including Prime Minister Narendra Modi have agreed to help to optimise the processes and procedures of the World Health Organization (WHO) for emergency use authorisation of Covid-19 vaccines, India's G20 Sherpa Piyush Goyal said
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WHO giving emergency use authorisation to Covaxin would facilitate process
Updated : 4 years, 4 months ago IST
Rome [Italy], October 31 (ANI): World Health Organisation giving approval for Emergency Use Authorisation for India's indigenous COVID-19 vaccine 'Covaxin' would facilitate the process of assisting other countries, Foreign Secretary Harsh Vardhan Shringla said on Saturday.
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WHO's emergency use authorisation for Covaxin further delayed: Sources
Updated : 4 years, 5 months ago IST
New Delhi [India], September 28 (ANI): The emergency use authorisation (EUA) for Bharat Biotech's COVID-19 vaccine Covaxin has once again been delayed by the World Health Organisation, said sources.
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