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Updated : 11 months, 2 weeks ago IST
Washington [US], December 18 (ANI): Advisors to the US Food and Drug Administration (FDA) voted in favour to recommend that the agency must give Emergency Use Authorisation (EUA) to Moderna's COVID-19 vaccine.
Updated : 11 months, 3 weeks ago IST
Washington [US], December 13 (ANI): Rival US companies UPS and FedEx are working side-by-side to ship the Pfizer-BioNTech Covid-19 vaccine, after it was approved for emergency use by the US Food and Drug Administration (FDA) on Friday.
Washington [US], December 12 (ANI): Soon after the US Food and Drug Administration on Friday approved Pfizer's COVID-19 vaccine for emergency use across the country, President Donald Trump said that the vaccine will be administered "in less than 24 hours."
New York [US], December 12 (ANI): The US Food and Drug Administration authorized Pfizer's Covid-19 vaccine for emergency use on Friday for the prevention of coronavirus disease in individuals 16 years of age and older.
Washington [US], December 11 (ANI): A panel of experts advising the US Food and Drug Administration (FDA) on Thursday recommended emergency approval for the Pfizer-BioNTech Covid-19 vaccine.
Updated : 1 year 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.
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
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.
Roorkee (Uttarakhand) [India], November 13 (ANI): Amid the rapid transmission of cases of Covid-19, a group of scientists from IIT Roorkee has leveraged Artificial Intelligence (AI) to predict 10 FDI (Food and Drug Administration) approved commercial drugs available for the treatment of the
Washington [US], November 12 (ANI): Moderna expects to have an announcement on the efficacy of its COVID-19 vaccine after it finished accumulating data for a first analysis of the vaccine, the company said in a statement on Wednesday.
Mumbai (Maharashtra) [India], November 11 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc., USA (Glenmark) has been granted final approval by the United States Food & Drug Administration (U.S. FDA) for Tacrolimus Capsules USP, 0.5 mg, 1 mg and 5 mg, the generic version of Prograf®1 C
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