RIO DE JANEIRO: A Brazilian association of private health clinics said Sunday that it was negotiating with the Indian pharmaceutical company Bharat Biotech to purchase five million doses of its Covid-19 vaccine, which India has just authorized for emergency use. The Brazilian Association of Vaccine Clinics (ABCVAC) confirmed on its …
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NEW DELHI: The Committee of Experts on Matter of the Central Organization for the Control of Medicines Standards on Friday has maintained that the data provided by Bharat Biotech for its coronavirus vaccine ‘Covaxin’ is not sufficient for the granting of emergency use approval and has asked for more information, …
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NEW DELHI: The drug regulator’s Subject Matter Expert Committee (SEC) on the Covid-19 vaccine sought more time to analyze updated data submitted by the Serum Institute of India and Bharat Biotech for emergency use authorization (USA ) for their respective SARS vaccine candidates. CoV2. The committee will meet again on …
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NEW DELHI: The countryfirst indigenous mRNA vaccine candidate developed by Gennova, Pune has received approval of drug regulators to initiate phase 1/2 human clinical trials, the Department of Biotechnology he said on Friday. The new mRNA candidate vaccine, HGCO19, is supported by an initial grant from the Ind-CEPI mission of …
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[ad_1] NEW DELHI: After direct foreign investment (FDI), the government is trying to stifle rampant access to the Indian market by Chinese portfolio investors as it seeks to fill a possible gap that border investors can use to acquire shares in listed national companies. The economic affairs department of the …
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[ad_1] Roche Holding AG has received emergency use approval from the United States Food and Drug Administration (FDA) for an antibody test to help determine if people have ever been infected with the coronavirus, the manufacturer said Sunday. Swiss drug. Governments, businesses, and individuals are looking for such blood tests, …
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[ad_1] The | Updated: Saturday May 2, 2020, 9:42 [IST] As the coronavirus pandemic continued to spread around the world, NASA halted its usual space-related activities and began developing a fan prototype to help combat the deadly virus. The newly developed fan has just received emergency approval from the US …
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[ad_1] U.S. regulators on Friday allowed emergency use of the first drug that appears to help some COVID-19 patients recover faster, a milestone in the global search for effective therapies against the coronavirus. The Food and Drug Administration said in a statement that Gilead Science’s intravenous drug would be specifically …
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[ad_1] Now, the state has requested and received ICMR approval to explore the feasibility of convalescent plasma transfusion. Kerala’s quick approach to defeating Covid-19 has yielded results showing the flattening of its infection curve, the highest recovery rate and low mortality. He was the first to decentralize surveillance and enable …
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[ad_1] File photo of the drug firm Cipla. (Photo courtesy: Cipla) The US Food and Drug Administration. USA It approved Indian drug maker Cipla Ltd to make the generic version of the albuterol sulfate-based inhaler in an attempt to help coronavirus patients. Reuters Last update: April 9, 2020, 11:42 a.m. …
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