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.
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.
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.
New Delhi [India], December 3 (ANI): The Indian Gas Exchange (IGX) said on Thursday it has secured necessary authorisation to operate as a gas exchange as per provisions of the Petroleum and Natural Gas Regulatory Board (Gas Exchange) Regulations 2020 for a period of 25 years.
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.
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
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.
New Delhi [India], September 18 (ANI): The government will allow private companies to utilise infrastructures of the Indian Space Research Organisation (ISRO), which are otherwise not available elsewhere in India under Indian National Space, Promotion and Authorisation Centre (INSPACe), said
Pune (Maharashtra) [India], Aug 31 (ANI/BusinessWire India): To simplify the process of authentication while selling shares from Demat Account, and to make it more secure, Bajaj Financial Securities Limited (BFSL) has implemented TPIN based verification in accordance with Central Depository
Washington D.C. [USA], July 19 (ANI): The US Food and Drug Administration (FDA) on Saturday (local time) issued an emergency use authorisation (EUA) to Quest Diagnostics that allows pool samples from up to four individuals to test for COVID-19.