Search For "authorisation"
Philippines FDA approves world's first generic version of Pfizer's anti-Co
Updated : 4 years, 1 month ago IST
Manila [Philippines], January 26 (ANI/PNN): The Philippines Food and Drug Administration (FDA) has approved the world's first generic version of Pfizer's anti-Coronavirus pill Paxlovid, just days after the original was granted Emergency Use Authorisation (EUA) by the US FDA.
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Novavax, Serum Institute file for emergency use authorisation of Novavax'
Updated : 4 years, 2 months ago IST
Gaithersburg [US], January 10 (ANI): Novavax, a biotechnology company dedicated to developing and commercializing next-generation vaccines for serious infectious diseases, and Serum Institute of India (SII), on Monday, announced a regulatory submission to the South African Health Products Re
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HDFC Bank goes live for customs duty payments
Updated : 4 years, 2 months ago IST
Mumbai (Maharashtra) [India], January 7 (ANI/BusinessWire India): HDFC Bank today announced that its integration with Central Board of Indirect Taxes and Customs (CBIC) ICEGATE platform has gone live. With this, the Bank will offer customers the convenience of directly paying Customs Duty by
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Covovax authorisation is a vital step in India, where additional vaccine o
Updated : 4 years, 2 months ago IST
Gaithersburg/Pune (Maryland/Maharashtra)[US/India], December 29 (ANI): Novavax, Inc. (Nasdaq: NVAX), a biotechnology company dedicated to developing and commercializing next-generation vaccines for serious infectious diseases, and Serum Institute of India (SII), the world's largest vaccin
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Dr Reddy's laboratories gets DCGI's nod to launch Molnupiravir capsules in
Updated : 4 years, 2 months ago IST
Hyderabad (Telangana) [India], December 28 (ANI): Drugs Controller General of India (DCGI) on Tuesday approved Dr Reddy's laboratories for the emergency-use authorisation) to manufacture and market the oral anti-viral drug Molnupiravir capsules 200mg for the treatment of adult patients with
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DCGI grants Cipla emergency use authorisation for COVID-19 drug Molnupirav
Updated : 4 years, 2 months ago IST
Mumbai (Maharashtra) [India], December 28 (ANI): Drug Controller General of India (DCGI) on Tuesday granted Emergency Use Authorisation (EUA) to Cipla for the launch of Molnupiravir in the country for COVID-19 treatment.
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US authorizes AstraZeneca's Evusheld for pre-exposure prevention of COVID-
Updated : 4 years, 3 months ago IST
New Delhi [India], December 9 (ANI): AstraZeneca's Evusheld (Tixagevimab co-packaged with Cilgavimab), a long-acting antibody (LAAB) combination, has received emergency use authorisation (EUA) in the US for the pre-exposure prophylaxis (prevention) of COVID-19, with first doses expected t
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Bharat Biotech's partner seeks Covaxin approval in US for children below 1
Updated : 4 years, 4 months ago IST
New Delhi [India], November 6 (ANI): Bharat Biotech's US partner Ocugen has announced that it had asked the US Food and Drug Administration (FDA) for Emergency Use Authorisation (EUA) of Covaxin for children below 18.
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UN Security Council extends authorisation of EU-led force in Bosnia and He
Updated : 4 years, 4 months ago IST
New York [US], November 4 (ANI/Xinhua): The United Nations Security Council on Wednesday extended the authorization of an EU-led peacekeeping force in Bosnia and Herzegovina (BiH) for another 12 months.
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G-20 leaders agreed to help optimise WHO procedures for Covid-19 vaccines
Updated : 4 years, 4 months ago IST
Rome [Italy], October 31 (ANI): Leaders of the G-20 nations including Prime Minister Narendra Modi have agreed to help to optimise the processes and procedures of the World Health Organization (WHO) for emergency use authorisation of Covid-19 vaccines, India's G20 Sherpa Piyush Goyal said
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WHO giving emergency use authorisation to Covaxin would facilitate process
Updated : 4 years, 4 months ago IST
Rome [Italy], October 31 (ANI): World Health Organisation giving approval for Emergency Use Authorisation for India's indigenous COVID-19 vaccine 'Covaxin' would facilitate the process of assisting other countries, Foreign Secretary Harsh Vardhan Shringla said on Saturday.
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US to put Sputnik V, other Vaccines on 'green' travel list after WHO autho
Updated : 4 years, 5 months ago IST
Washington [US], October 26 (ANI/Sputnik): The United States will add foreign COVID-19 vaccines, including Russia's Sputnik V, to its list of accepted shots upon authorization by the World Health Organization (WHO), the Centers for Disease Control (CDC) Travelers' Health Branch Chief Cindy F
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