Pune (Maharashtra) [India], December 28 (ANI): Serum Institute of India on Tuesday expressed gratitude to the Union Health Ministry for granting Emergency Use Authorization for its COVID-19 vaccine Covovax.
Seoul [South Korea], December 28 (ANI/Global Economic): 'Paxlovid,' the COVID-19 oral treatment developed by a global pharmaceutical company Pfizer, received emergency use authorization from the Ministry of Food and Drug Safety (MFDS) on the 27th. It is expected to be used from the end of Ja
New Delhi [India], December 28 (ANI): After reviewing all applications and data, the Subject Expert Committee (SEC), a body under India's drug regulator, has recommended granting the Emergency Use Authorization (EUA) to Serum Institute of India's COVID-19 vaccine Covovax and Corbevax vacc
Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Thursday said that it has granted an emergency use authorization for Merck's antiviral pill Molnupiravir that is used to treat COVID-19 patients.
Washington [US], November 19 (ANI): The US Food and Drug Administration on Friday (local time) expanded the emergency use authorization (EUA) for the Pfizer and Moderna COVID-19 vaccine boosters signaling that the shots can be given to anyone aged 18+ at least six months after completion of
Rome [Italy], October 30 (ANI): Prime Minister Narendra Modi conveyed to leaders of G20 nations that India is ready to produce five billion COVID-19 vaccines doses by the end of 2022, Foreign Secretary Harsh Vardhan Shringla said on Saturday.
Geneva [Switzerland], October 5 (ANI): World Health Organisation (WHO) has extended giving the emergency use authorization for Hyderabad-based Bharat Biotech's COVID-19 vaccine Covaxin to next week.
New Delhi [India], September 24 (ANI): The Union Health Ministry on Friday hinted that World Health Organization's emergency use authorization to Covaxin is expected soon.
Hyderabad (Telangana) [India], September 6 (ANI): Hetero announced on Monday that the Drug Controller General of India (DCGI) has approved Emergency Use Authorization (EUA) for its generic version of Tocilizumab in India for the treatment of COVID-19 in hospitalised adults.
Moscow [Russia], August 23 (ANI): The Philippines' Food and Drug Administration approved the single-component Sputnik Light coronavirus vaccine under the emergency use authorization procedure on Monday, the Russian Direct Investment Fund said.
New Delhi [India], August 7 (ANI): US pharma giant Johnson and Johnson's single-dose COVID-19 vaccine Janssen has received approval for Emergency Use Authorization (EUA) in India, informed Union Health Minister Mansukh Mandaviya on Saturday.
New Delhi [India], August 6 (ANI): US pharma giant Johnson and Johnson on Friday said it has applied for Emergency Use Authorization (EUA) of its single-dose COVID-19 vaccine Janssen to the Government of India.