Emergency Use Of Covid-19 Vaccine
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India's Corbevax Vaccine Gets WHO Emergency Use Listing Authorisation
India's COVID-19 vaccine, Corbevax, has been granted an Emergency Use Listing by the World Health Organisation, the company which manufactures it in India said Hyderabad today.
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Gennova mRNA Covid Booster Vaccine Gets Emergency Use Authorisation
Pune-based Gennova Biopharmaceuticals Ltd on Tuesday said its mRNA COVID-19 booster vaccine against the Omicron variant, GEMCOVAC-OM, has received emergency use authorisation from the Drugs Controller General of India.
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Serum Institute's Covid Vaccine Covovax Cleared For 7-11 Age Group
The Drugs Controller General of India (DCGI) on Tuesday approved Serum Institute's COVID-19 vaccine Covovax for restricted emergency use in children aged 7 to 11 years subject to certain conditions, official sources said.
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US Approves Covid Vaccine For Children 6 Months And Above
The US Food and Drug Administration granted emergency authorization Friday for the use of Pfizer and Moderna Covid-19 vaccines in the youngest children, the final age group awaiting immunization in most countries.
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Novavax's Covid Vaccine Gets Emergency Use Nod For Kids Aged 12-17 In India
Novavax Inc said on Tuesday its COVID-19 vaccine has got emergency-use authorization from the Drugs Controller General of India for children aged 12 to 17 years.
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Covovax Gets Emergency Use Approval For Children Above 12 Years
India's drug regulator has granted restricted emergency use authorisation to Serum Institute of India's COVID-19 vaccine Covovax for the 12-17 years age group subject to certain conditions, official sources said on Wednesday.
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One-Shot Sputnik Light Vaccine Gets Emergency Use Approval In India
The Drugs Controller General of India (DCGI) has granted emergency-use permission to the single-dose Sputnik Light COVID-19 vaccine, informed Union Health Minister Mansukh Mandaviya on Sunday.
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Serum Institute Seeks Emergency Use Approval Of Covid Vaccine Covovax In South Africa
Novavax and Serum Institute of India (SII) announced a regulatory submission to the South African Health Products Regulatory Agency for emergency use authorization (EUA) of Novavax' recombinant nanoparticle protein-based COVID-19 vaccine
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Serum Institute Thanks Centre For Emergency Use Approval For Covovax
Serum Institute of India on Tuesday expressed gratitude to the Union Health Ministry for granting Emergency Use Authorization for its COVID-19 vaccine Covovax.
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Covaxin Cleared For Children Above 12 By Drug Regulator
Bharat Biotech's COVID-19 vaccine Covaxin has been approved for emergency use on children between the ages of 12 and 18 by the Drugs Controller General of India (DCGI), sources said.
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UK To Recognise Covaxin, No Quarantine For Fully Vaccinated Travellers
Britain said it would recognise COVID-19 vaccines on the World Health Organization's Emergency Use Listing later this month, adding China's Sinovac, Sinopharm and India's Covaxin to the country's approved list of vaccines for inbound travellers.
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WHO's Covaxin Approval Will Facilitate Travel For Indians: S Jaishankar
External Affairs Minister S Jaishankar on Wednesday said the WHO''s decision to grant emergency use approval to Bharat Biotech''s COVID-19 vaccine Covaxin facilitates travel for many Indian citizens and contributes to vaccine equity.
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WHO In Talks With Covaxin Maker Bharat Biotech To Join Its Tech Access Pool: Official
The World Health Organisation is in negotiations with Bharat Biotech, whose COVID-19 vaccine Covaxin was given Emergency Use Listing, to join the global health agency's technology access pool to share technology and know how, a top WHO official said
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Approval To Covaxin Expands Availability Of Vaccines, Says WHO Official
The Emergency Use Listing nod to Bharat Biotech's Covaxin, which was found to have 78 per cent efficacy against COVID-19 of any severity, expands the availability of vaccines, the most effective medical tools to end the pandemic, a WHO official said
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Novavax-Serum Institute Vaccine Gets Emergency Use Approval In Indonesia
Biotechnology firm Novavax Inc and its partner Serum Institute of India on Monday said they have received the first emergency use authorisation (EUA) for Novavax''s COVID-19 vaccine, in Indonesia.
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India's Corbevax Vaccine Gets WHO Emergency Use Listing Authorisation
India's COVID-19 vaccine, Corbevax, has been granted an Emergency Use Listing by the World Health Organisation, the company which manufactures it in India said Hyderabad today.
-
Gennova mRNA Covid Booster Vaccine Gets Emergency Use Authorisation
Pune-based Gennova Biopharmaceuticals Ltd on Tuesday said its mRNA COVID-19 booster vaccine against the Omicron variant, GEMCOVAC-OM, has received emergency use authorisation from the Drugs Controller General of India.
-
Serum Institute's Covid Vaccine Covovax Cleared For 7-11 Age Group
The Drugs Controller General of India (DCGI) on Tuesday approved Serum Institute's COVID-19 vaccine Covovax for restricted emergency use in children aged 7 to 11 years subject to certain conditions, official sources said.
-
US Approves Covid Vaccine For Children 6 Months And Above
The US Food and Drug Administration granted emergency authorization Friday for the use of Pfizer and Moderna Covid-19 vaccines in the youngest children, the final age group awaiting immunization in most countries.
-
Novavax's Covid Vaccine Gets Emergency Use Nod For Kids Aged 12-17 In India
Novavax Inc said on Tuesday its COVID-19 vaccine has got emergency-use authorization from the Drugs Controller General of India for children aged 12 to 17 years.
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Covovax Gets Emergency Use Approval For Children Above 12 Years
India's drug regulator has granted restricted emergency use authorisation to Serum Institute of India's COVID-19 vaccine Covovax for the 12-17 years age group subject to certain conditions, official sources said on Wednesday.
-
One-Shot Sputnik Light Vaccine Gets Emergency Use Approval In India
The Drugs Controller General of India (DCGI) has granted emergency-use permission to the single-dose Sputnik Light COVID-19 vaccine, informed Union Health Minister Mansukh Mandaviya on Sunday.
-
Serum Institute Seeks Emergency Use Approval Of Covid Vaccine Covovax In South Africa
Novavax and Serum Institute of India (SII) announced a regulatory submission to the South African Health Products Regulatory Agency for emergency use authorization (EUA) of Novavax' recombinant nanoparticle protein-based COVID-19 vaccine
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Serum Institute Thanks Centre For Emergency Use Approval For Covovax
Serum Institute of India on Tuesday expressed gratitude to the Union Health Ministry for granting Emergency Use Authorization for its COVID-19 vaccine Covovax.
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Covaxin Cleared For Children Above 12 By Drug Regulator
Bharat Biotech's COVID-19 vaccine Covaxin has been approved for emergency use on children between the ages of 12 and 18 by the Drugs Controller General of India (DCGI), sources said.
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UK To Recognise Covaxin, No Quarantine For Fully Vaccinated Travellers
Britain said it would recognise COVID-19 vaccines on the World Health Organization's Emergency Use Listing later this month, adding China's Sinovac, Sinopharm and India's Covaxin to the country's approved list of vaccines for inbound travellers.
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WHO's Covaxin Approval Will Facilitate Travel For Indians: S Jaishankar
External Affairs Minister S Jaishankar on Wednesday said the WHO''s decision to grant emergency use approval to Bharat Biotech''s COVID-19 vaccine Covaxin facilitates travel for many Indian citizens and contributes to vaccine equity.
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WHO In Talks With Covaxin Maker Bharat Biotech To Join Its Tech Access Pool: Official
The World Health Organisation is in negotiations with Bharat Biotech, whose COVID-19 vaccine Covaxin was given Emergency Use Listing, to join the global health agency's technology access pool to share technology and know how, a top WHO official said
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Approval To Covaxin Expands Availability Of Vaccines, Says WHO Official
The Emergency Use Listing nod to Bharat Biotech's Covaxin, which was found to have 78 per cent efficacy against COVID-19 of any severity, expands the availability of vaccines, the most effective medical tools to end the pandemic, a WHO official said
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Novavax-Serum Institute Vaccine Gets Emergency Use Approval In Indonesia
Biotechnology firm Novavax Inc and its partner Serum Institute of India on Monday said they have received the first emergency use authorisation (EUA) for Novavax''s COVID-19 vaccine, in Indonesia.
