New Delhi [India], April 13 (ANI): The Central government has fast-tracked emergency approvals for foreign-produced COVID-19 vaccines that have been granted Emergency Use Authorization (EUA) in other countries to expand the basket of vaccines for domestic use and hasten the pace and coverage
New Delhi [India], April 12 (ANI): Russia's Sputnik V got approval from the Subject expert committee (SEC) for Emergency Use Authorisation (EUA), making it the third Covid-19 vaccine to get clearance in India.
New Delhi [India], April 12 (ANI): The Subject Expert Committee (SEC) is likely to meet today to take up Sputnik V application for Emergency Use Authorisation (EUA) in India, said sources.
New Delhi [India], April 1 (ANI): Russia's COVID-19 Sputnik V vaccine was denied emergency use authorisation in India on Thursday by the Subject Expert Committee (SEC) constituted by the central government.
Washington DC [US], March 10 (ANI): 340 different coronavirus tests have so far won emergency use authorisation (EUA), including one that can be used at home without a prescription to detect the virus, the Food and Drug Administration (FDA) has said.
New Delhi [India], February 24 (ANI): The Central Drugs Standard Control Organisation's (CDSCO) Subject Expert Committee (SEC) has recommended additional immunogenicity data from Dr Reddy's Laboratories which applied to the national drugs regulator seeking emergency use approval for Sputnik
New Delhi [India], February 24 (ANI): The Central Drugs Standard Control Organisation's (CDSCO) Subject Expert Committee (SEC) is going to meet on Wednesday afternoon to discuss Dr Reddy's Laboratories application seeking emergency use approval (EUA) for SputnikV, a Russian Vaccine.
Geneva [Switzerland], February 16 (ANI): The World Health Organisation (WHO) on Monday (local time) gave emergency use approval (EUA) to two versions of AstraZeneca-Oxford-developed COVID-19 vaccines, allowing these shots to be rolled out globally through COVAX. The vaccines are being produc
New Delhi [India], January 5 (ANI): Days after Drugs Controller General of India (DCGI) gave approval to two COVID-19 vaccines, Union Health Secretary Rajesh Bhushan on Tuesday said that India is prepared to roll out vaccine within 10 days of emergency use authorisation (EUA), subject to
New Delhi [India], January 2 (ANI): Various editions of Urdu publications have carried the prominent news that the Subject Expert Committee of Drugs Controller General of India (DCGI) has recommended granting permission for Emergency Use Authorisation (EUA) with certain conditions to COVID-1
New Delhi [India], January 1 (ANI) In a major development related to the COVID vaccine, the Subject Expert Committee of Drugs Controller General of India (DCGI) has recommended granting permission for Emergency Use Authorisation (EUA)with certain conditions to COVID-19 vaccine being manufact
New Delhi [India], December 24 (ANI/NewsVoir): It's been a year now since the first few human cases of COVID-19 infection were reported amidst the busy wholesale food market of China's Wuhan city. The disease caused by SARS-CoV-2 virus, thought to have its origin in Bats, soon spread to caus