Search For "emergency use"
Bharat Biotech applies for emergency use authorisation for its COVID-19 va
Updated : 5 years, 5 months ago IST
New Delhi [India], December 7 (ANI): Bharat Biotech on Monday applied for emergency use authorisation for its indigenously developed COVID-19 vaccine 'Covaxin' to Drugs Controller General of India (DCGI), officials said.
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SII CEO thanks PM Modi for support after seeking emergency authorisation o
Updated : 5 years, 5 months ago IST
New Delhi [India], December 7 (ANI): After Serum Institute India (SII) applied for the emergency use authorisation of its coronavirus vaccine "COVISHIELD", its CEO Adar Poonawala expressed gratitude to Prime Minister Narendra Modi and the central government for the support.
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Serum Institute of India seeks emergency use authorisation for its COVID-1
Updated : 5 years, 5 months ago IST
New Delhi [India], December 7 (ANI): The Serum Institute of India (SII) has applied to the Drugs Controller General of India (DCGI) seeking emergency use authorisation for its COVID-19 vaccine "Covishield" in the country.
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Pfizer becomes first pharma company in India to seek emergency use nod for
Updated : 5 years, 5 months ago IST
New Delhi [India], December 6 (ANI): Pfizer India has become the first pharmaceutical firm to approach the Drugs Controller General of India (DCGI) seeking an emergency use authorisation for its Covid-19 vaccine in the country.
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Hopeful India will get Covid-19 vaccine nod by Dec end or early Jan: AIIMS
Updated : 5 years, 5 months ago IST
New Delhi [India], December 3 (ANI): Director of the All Indian Institute of Medical Sciences (AIIMS) Dr Randeep Guleria has said that he is hopeful of that by the end of this month or early next month, India will get emergency use authorisation for a coronavirus vaccine.
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COVID-19: Moderna submits vaccine data to obtain emergency use authorisati
Updated : 5 years, 5 months ago IST
Washington DC [US], December 1 (ANI): US biotech company Moderna said that it has submitted the results of its coronavirus vaccine trials to the country's Food and Drug Administration (FDA) in order to obtain emergency use authorisation for the vaccine.
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Moderna to request Emergency use authorisation, its vaccine 100% effective
Updated : 5 years, 5 months ago IST
Washington [US], November 30 (ANI): US biotech company Moderna on Monday announced that it plans to request an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) and conditional approval from the European Medicines Agency (EMA) after the final results from a lat
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WHO interested in best practices, clinical data on vaccines getting emerge
Updated : 5 years, 5 months ago IST
Geneva [Switzerland], November 28 (ANI/Sputnik): Mariangela Simao, the World Health Organization's (WHO) assistant director-general for access to medicines and health products, said on Friday that the exchange of clinical data and best practices of COVID-19 vaccine manufacturing remained cru
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Pfizer, BioNTech to submit to FDA for emergency use authorisation for thei
Updated : 5 years, 6 months ago IST
Washington [US], November 20 (ANI): American drug giant Pfizer and German laboratory BioNTech on Friday said that they will be submitting to the US Food and Drug Administration for emergency use authorisation for their COVID-19 vaccine candidate.
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May recommend Russian vaccine for emergency use if criteria met: WHO
Updated : 5 years, 6 months ago IST
Geneva [Switzerland], November 12 (ANI/Sputnik): The World Health Organization (WHO) may add Russian coronavirus vaccine Sputnik V to the list of recommended vaccines for emergency use if the candidate meets necessary criteria, it has told Sputnik in a statement.
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US allows emergency use of Eli Lilly's COVID-19 antibody treatment
Updated : 5 years, 6 months ago IST
Washington DC [US], November 10 (ANI): The US Food and Drug Administration (FDA) has approved an emergency use authorisation (EUA) for American pharmaceutical company Eli Lilly's experimental COVID-19 antibody treatment called 'bamlanivimab' for non-hospitalised patients with mild-to-moderat
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WHO to soon issue guidelines on use of emergency drug Remdesivir
Updated : 5 years, 7 months ago IST
Geneva [Switzerland], October 17 (ANI): The World Health Organization is set to issue policy guidelines in several weeks on the use of the antiviral drug Remdesivir, which has been given in emergency use to treat COVID-19 in several countries.
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