FDA approves saliva-based coronavirus test viewed as 'major game changer'
Aug 15, 2020
The Food and Drug Administration on Saturday issued an emergency use authorization for the SalivaDirect COVID-19 diagnostic test developed by the Yale School of Public Health.
The test, which processes saliva samples to rapidly determine whether a person is infected with the coronavirus and does not require any type of swab or specific collection device, could be one of the first "major game changers in fighting the pandemic," said Andy Slavitt, a former acting administrator of the Centers for Medicare and Medicaid Services under the Obama administration, in a Twitter thread.
For starters, the process should be a lot more comfortable for people.
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