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    • AUGUST 25, 2020
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    Coronavirus (COVID-19) | FDA News Release | FDA Issues Emergency Use Authorization to Yale School of Public Health for SalivaDirect, Which Uses a New Method of Saliva Sample Processing

    Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) to Yale School of Public Health for its SalivaDirect COVID-19 diagnostic test, which uses a new method of processing saliva samples when testing for COVID-19 infection. “The SalivaDirect test for rapid detection of SARS-CoV-2 is yet another testing innovation game changer that will

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    • Hassan Nadrous
    • Coronavirus (SARS-CoV-2) | COVID-19,
    • FDA News Release
    • OCTOBER 23, 2020
    • 0

    COVID-19 Update | FDA News Release | FDA Issues Emergency Use Authorization for Convalescent Plasma as Potential Promising COVID–19 Treatment, Another Achievement in Administration’s Fight Against Pandemic

    Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for investigational convalescent plasma for the treatment of COVID-19 in hospitalized patients as part of the agency’s ongoing efforts to fight COVID-19. Based on scientific evidence available, the FDA concluded, as outlined in its decision memorandum, this product may be effective in treating

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    • Hassan Nadrous
    • Coronavirus (SARS-CoV-2) | COVID-19,
    • FDA News Release

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  • COVID-19 | Medical Editorial | Convalescent plasma is ineffective for covid-19 October 23, 2020
  • COVID-19 | Medical Research Study | Convalescent plasma in the management of moderate covid-19 in adults in India: open label phase II multicentre randomised controlled trial (PLACID Trial) October 23, 2020
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