New Delhi [India], May 8 (ANI): The Drugs Controller General of India (DCGI) has approved the emergency use of an anti-COVID drug - 2-deoxy-D-glucose (2-DG) - as an adjunct therapy in moderate to severe COVID-19 cases.
Geneva [Switzerland], May 8 (ANI): The World Health Organisation (WHO) on Friday approved the Chinese Sinopharm COVID-19 vaccine for emergency use, paving the way for it to be rolled out globally.
Washington [US], May 7 (ANI): Pharmaceutical giants Pfizer and BioNTech on Friday said that they have started the process for getting the US Food and Drug Administration (FDA) complete authorisation of its COVID-19 vaccine after having emergency use authorization for almost five months.
Geneva [Switzerland], May 1 (ANI): The World Health Organization (WHO) on Friday listed the Moderna coronavirus vaccine for emergency use, adding another shot to its arsenal in the fight against the coronavirus.
Dhaka [Bangladesh], April 28 (ANI): The Directorate General of Drug Administration (DGDA) of Bangladesh has green-lit the emergency use of Russia's Sputnik V COVID-19 vaccine, the second vaccine to be used in the country.
Gurugram (Haryana) [India], April 24 (ANI): Amid an acute shortage of oxygen due to the second wave of the coronavirus pandemic, SpiceXpress, the air cargo arm of SpiceJet, airlifted 800 oxygen concentrators from Hong Kong for emergency use and distribution across the country.
New Delhi [India], April 23 (ANI): Zydus Cadila received emergency use approval from the Drugs Controller General of India (DGCI) on Friday for the use of 'Virafin', Pegylated Interferon alpha-2b (PegIFN) in treating moderate COVID-19 infection in adults.
New Delhi [India], April 23 (ANI): The Drugs Controller General of India (DGCI) has approved emergency use for Zydus Cadila's Pegylated Interferon alpha-2b, 'Virafin' for treating moderate COVID-19 infection in adults.
New Delhi [India], April 15 (ANI): In view of the rapid surge in coronavirus cases in India, the Central government approved a significant streamlining and fast-tracking of the regulatory system for COVID-19 vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which ar
New Delhi [India], April 15 (ANI): The Central Government on Thursday issued the regulatory pathway in India for COVID-19 vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which are listed in WHO Emergency Use Listing (EUL), said the Union Health Ministry.
New Delhi [India], April 14 (ANI): Congress leader Rahul Gandhi on Wednesday took a jibe at the central government after it granted permission for emergency use authorisation of Sputnik-V, the Russian vaccine against COVID-19.
New Delhi [India], April 14 (ANI): Roman Babushkin, Russian Deputy Envoy to India on Wednesday said that Sputnik vaccine emergency use approval by India will open up a new dimension in the special partnership.