Quick and affordable saliva-based COVID-19 test developed by Yale scientists received FDA Emergency Use Authorization

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On Aug. 15, 2020, a saliva-based laboratory diagnostic test developed by researchers at the Yale School of Public Health to determine whether someone is infected with the novel coronavirus was granted an emergency use authorization by the FDA.

The method, called SalivaDirect, is being further validated as a test for asymptomatic individuals through a program that tests players and staff from the National Basketball Association. SalivaDirect is simpler, less expensive, and less invasive than the traditional method for such testing, known as nasopharyngeal (NP) swabbing.

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Source: Yale School of Public Health
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