The head of India’s drug regulator will deliver a press conference on Sunday, a day after his experts recommended allowing the emergency use in the country of the Oxford-AstraZeneca and Bharat Biotech vaccines against the coronavirus disease ( Covid-19), according to reports. . The Comptroller General of Drugs of India …
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An expert panel from India’s top drug regulator on Saturday recommended restricted emergency approval for Covaxin, Bharat Biotech’s Covid-19 candidate vaccine currently being tested in the country. The panel of experts now recommended a restricted authorization for two candidate vaccines in as many days; on Friday, it recommended similar approval …
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Bharat Biotech vaccine candidate approved for use in clinical trial mode. The first COVID-19 vaccine developed in India, Covaxin, has been recommended for “restricted use in emergency situations, subject to multiple regulatory conditions” by the Subject Matter Expert Committee (SEC) of the Central Medicines Control Organization ( CDSCO), here on …
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An expert panel from India’s central drug authority on Saturday recommended granting permission for the restricted use of the indigenous COVID-19 vaccine developed by Bharat Biotech Covaxin in an emergency situation, especially in the context of infection by mutant strains, authorities said. The recommendation for the Bharat Biotech vaccine came …
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NEW DELHI: An expert panel from India’s drug authority recommended Saturday restricted emergency use of Bharat Biotechis Covaxin. The development comes one day after the recommended panel. emergency use authorization for the Serum Institute of India’s (SII) Covishield. The Central Medicines Control Organization (CDSCO) Subject Matter Expert Committee (SEC) on …
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Covaxin has been indigenously developed in collaboration with ICMR. An expert panel from India’s central drug authority recommended on January 2 to grant permission for the emergency restricted use of the locally developed COVID-19 vaccine Covaxin with certain conditions, a day after giving similar instructions for the COVID vaccine. -19 …
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NEW DELHI: The Subject Matter Expert Committee (SEC) of the national drug regulator is likely to hold a meeting with Bharat Biotech on Saturday to consider your Covid-19 vaccine applicant, Covaxin. The committee constituted by the Central Organization for the Control of Medicines Standards on Friday had held that the …
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A committee of experts from the country’s top drug regulator recommended on Friday that Covishield, the Indian version of the Covid-19 vaccine developed by the University of Oxford and AstraZeneca, should be approved under certain conditions, The Indian Express has learned. The recommendation is hugely significant as it paves the …
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India will hold a trial on Saturday before the actual vaccination campaign against the coronavirus disease (Covid-19) in an end-to-end exercise in which all steps will be tested in the states and territories of the Union. The activity will take place in all state capitals at at least three session …
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A government panel of experts reportedly approved the vaccine, developed by AstraZeneca and the University of Oxford, for emergency use in India to provide immunity against coronavirus disease (Covid-19). According to the Reuters news agency, a committee of experts in the field, created by the Comptroller General of Drugs of …
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