Search For "emergency use"
Bharat Biotech, WHO pre-submission meeting on June 23: WHO
Updated : 4 years, 11 months ago IST
New Delhi [India], June 17 (ANI): Hyderabad-based Bharat Biotech's pre-submission meeting has been scheduled on June 23 for evaluation of the World Health Organisation (WHO)'s Emergency Use Listing (EUL) of its indigenous COVID-19 vaccine Covaxin.
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We respect US FDA decision, but it won't impact India's vaccine plan: Cent
Updated : 4 years, 11 months ago IST
New Delhi [India], June 11 (ANI): Reacting to the United States Food and Drug Administration (FDA)'s rejection of Bharat Biotech's Covaxin jab for emergency use authorization, the Union Health Ministry on Friday said that it respects the decision taken by the authority but it will not hav
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Bharat Biotech's US partner, Ocugen to apply for full approval for Covaxin
Updated : 4 years, 11 months ago IST
Pennsylvania [US], June 11 (ANI): Bharat Biotech's US partner Ocugen Inc said that the company will no longer pursue an Emergency Use Authorization (EUA) for COVAXIN and the US Food and Drug Administration (FDA) has recommended that the company go for the Biologics Licence Application (BL
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Centre issues guidelines for COVID management in children, discourages use
Updated : 4 years, 11 months ago IST
New Delhi [India], June 10 (ANI): The Director General of Health Services (DGHC) under the Union Health Ministry on Wednesday issued guidelines for the management of COVID-19 in children below 18 years of age, according to which use of Remdesivir, an emergency use authorisation drug, has
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COVID-19: WHO approves emergency use of China's CoronaVac vaccine
Updated : 4 years, 11 months ago IST
Geneva [Switzerland], June 1 (ANI): The World Health Organisation (WHO) on Tuesday approved the Chinese COVID-19 vaccine CoronaVac for emergency use, the second Chinese vaccine to receive the global health body's green light.
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Biological E ties up with Canada's Providence to produce mRNA COVID-19 vac
Updated : 4 years, 11 months ago IST
Hyderabad (Telangana) [India], June 1 (ANI): Biological E. Limited has tied up with Canada's Providence Therapeutics to locally manufacture its mRNA coronavirus disease (COVID-19) vaccine, the Hyderabad-based company announced on Tuesday, adding it will run a pivotal trial in India, and seek
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Eli Lilly's antibody cocktail drug gets emergency use nod in India
Updated : 4 years, 11 months ago IST
New Delhi [India], June 1 (ANI): Eli Lilly and Company India on Tuesday announced that it has received emergency use approval in the country for its monoclonal antibody drug combination used for treating Covid-19 patients with mild to moderate symptoms.
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2DG approved for emergency use as adjunct therapy for COVID-19 patients: D
Updated : 4 years, 11 months ago IST
New Delhi [India], June 1 (ANI): The Defence Research and Development Organisation's (DRDO) on Tuesday said that the anti-COVID drug 2DG is approved for emergency use as an adjunct therapy to the standard of care in the treatment of coronavirus patients in hospital settings.
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Lilly India gets nod for use of monoclonal antibody drugs for treating Cov
Updated : 4 years, 11 months ago IST
New Delhi [India], June 1 (ANI): Eli Lilly and Company India said on Tuesday it has received permission for restricted emergency use of its antibody drugs bamlanivimab 700 mg and etesevimab 1,400 mg in India for treatment of patients with mild to moderate coronavirus disease 2019 (Covid-19).
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Bharat Biotech says EUL for COVAXIN submitted to WHO, approval expected by
Updated : 4 years, 12 months ago IST
New Delhi [India], May 26 (ANI): COVID-19 vaccine COVAXIN's manufacturer Bharat Biotech on Tuesday said application for Emergency Use Listing (EUL) of its vaccine has been submitted to World Health Organisation (WHO), Geneva, and regulatory approvals are expected between July and Septembe
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Bharat Biotech submits 90 pc documentation, confident of WHO emergency use
Updated : 4 years, 12 months ago IST
New Delhi [India], May 24 (ANI): Bharat Biotech is confident about obtaining the World Health Organization's (WHO) Emergency Use Listing for its COVID-19 vaccine given its experience of getting its other vaccines pre-qualified and has submitted 90 per cent of the documentation required for E
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US FDA approves emergency use of Pfizer-BioNTech vaccine for children in 1
Updated : 5 years ago IST
Washington [US], May 11 (ANI): The US Food and Drug Administration (FDA) on Monday (local time) authorised the emergency use of the Pfizer-BioNTech COVID-19 vaccine to children in the age group of 12-15 years.
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