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 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
London [UK], October 24 (ANI): The clinical trials for the AstraZeneca Oxford coronavirus vaccine -- AZD1222 -- have resumed in the United States after approval by the Food and Drug Administration (FDA), the company said on Friday (local time).
Washington [US], October 23 (ANI): The United States Food and Drug Administration (FDA) has approved Remdesivir for the treatment of coronavirus, Al Jazeera reported citing a statement issued by Gilead Sciences, Inc.
New Delhi [India], Sep 26 (ANI): The global demand scenario for Indian pharmaceutical industry is largely expected to remain stable due to inelastic nature of prescription drugs, investment information agency ICRA has said.
Washington [US], September 24 (ANI/Sputnik): US President Donald Trump ON Wednesday (local time) said that his administration may or may not approve a proposal from the Food and Drug Administration (FDA) that would tighten guidelines for approving a novel coronavirus disease (COVID-19) vacci
Mumbai (Maharashtra) [India], Aug 24 (ANI): Equity benchmark indices traded on a positive note during early hours on Monday led by gains in financial and auto stocks.
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.
Washington [US], Aug 23 (ANI): US President Donald Trump on Saturday (local time) slammed the Food and Drug Administration (FDA) for trying to slow down the human trials of coronavirus vaccines.
Washington [US], August 16 (ANI/Sputnik): The United States' Food and Drug Administration (FDA) has approved a new COVID-19 testing method based on analysing saliva samples.
Noida (Uttar Pradesh) [India], Aug 4 (ANI): Jubilant Life Sciences has launched Remdesivir for injection under the brand name JUBI-R in Indian market at a price of Rs 4,700 per vial of 100 mg and said it will make the drug available to over 1,000 hospitals providing COVID-19 treatment throug