Search For "authorization"
Pfizer withdraws emergency use request for its COVID vaccine in India
Updated : 5 years, 1 month ago IST
New Delhi [India], February 5 (ANI): US-based pharma company Pfizer has withdrawn an application for emergency-use authorization of its COVID-19 vaccine in India, the company spokesperson said.
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Enzene Biosciences Ltd. obtains marketing authorization for its first bios
Updated : 5 years, 1 month ago IST
Pune (Maharashtra) [India], February 4 (ANI/PRNewswire): Recently Enzene Biosciences Ltd. announced that it has obtained Marketing Authorisation (MA) from Drug Controller General of India (DCGI) for Teriparatide - bioactive part of human parathyroid hormone (PTH), an anabolic approach to the
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Indians are not guinea pigs, you can't use Covaxin rollout as phase 3 tria
Updated : 5 years, 2 months ago IST
New Delhi [India], January 14 (ANI): Congress leader Manish Tewari on Wednesday said that emergency use authorization to COVID-19 vaccine 'Covaxin' raises concerns on its efficacy as phase three trials have not been completed and its roll out can't be used as phase three trial. He said India
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McConnell says US Senate will vote to override Trump veto of Defense Bill
Updated : 5 years, 2 months ago IST
Washington DC [US], December 30 (ANI/Sputnik): The US Senate will vote on Wednesday to override President Donald Trump's veto of the fiscal year 2021 National Defense Authorization Act (NDAA), Senate Majority Leader Mitch McConnell said during remarks on the Senate floor on Tuesday.
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Regulators looking into emergency use authorization sought by Pfizer for C
Updated : 5 years, 2 months ago IST
New Delhi [India], December 21 (ANI): Union Health Minister Dr Harsh Vardhan has said that regulators are examining the permission sought by the Indian arm of US pharmaceutical firm Pfizer for emergency authorization of its Covid-19 vaccine.
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US allocates 2 million doses of Pfizer's Covid-19 vaccines for next week
Updated : 5 years, 2 months ago IST
Washington [US], December 16 (ANI/Sputnik): The US government has allocated 2 million doses of Pfizer's coronavirus vaccine to jurisdictions in the United States and almost 6 million doses of the Moderna coronavirus vaccine in case it receives the necessary authorization, Health and Human Se
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White House advised to veto National Defense Authorization Act
Updated : 5 years, 3 months ago IST
Washington [US], December 9 (ANI/Sputnik): The White House Office of Management and Budget in a letter said US President Donald Trump has been advised to veto the revised 2021 National Defense Authorization Act (NDAA).
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COVID-19: Moderna submits vaccine data to obtain emergency use authorisati
Updated : 5 years, 3 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, 3 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, 3 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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Drugs regulator refuses application of Dr Reddy's Lab for marketing author
Updated : 5 years, 4 months ago IST
New Delhi [India], November 2 (ANI): The top drug regulator has refused Dr Reddy's Laboratories' application, for full marketing authorization of anti-viral drug Remdesivir, for treatment of COVID-19 patients in India.
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Trump announces emergency authorization of convalescent plasma to treat C
Updated : 5 years, 6 months ago IST
Washington D.C. [US], August 24 (ANI): The US Food and Drug Administration (FDA) has authorised the use of convalescent plasma for the treatment of COVID-19 patients.
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