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FDA Emergency Use Authorized

A rapid serology test for the qualitative detection of SARS-CoV-2 IgG and IgM antibodies in venous whole blood, serum and plasma

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News

Jun 12, 2020

NCI Evaluation of COVID-19 Tests

The FDA worked with a number of agencies in efforts to evaluate the sensitivity and specificity of various COVID-19 serology tests. Test ...

Jun 11, 2020

COVID-19 IgG/IgM EUA

Breaking News: As of May 29,2020 the U.S. Food and Drug Administration (FDA) has provided Emergency Use Authorization (EUA) for the Healg...