Individual Saliva Test for COVID-19 Approved for Emergency Use Authorization by FDA
Governor Andrew M. Cuomo and State University of New York Chancellor Jim Malatras announced that the individual saliva swab diagnostic test for COVID-19 developed by SUNY Upstate Medical University and Quadrant Biosciences has been granted emergency use authorization by the U.S. Food and Drug Administration. While this test has been used to date to support SUNY's widespread testing of students across campuses, the emergency use authorization will help additional labs begin to use this test, helping pinpoint and contain the virus and protect New Yorkers.
The FDA-authorized saliva test for individuals complements Upstate Medical's and Quadrant's innovative pool testing, which allows for about 10 to 25 people to be screened in one COVID-19 test. The test's approval by the FDA means it can be brought to scale across New York State as well as used nationwide.
The approved tests can be conducted using saliva swabs rather than swabs inserted in a person's nose. Individuals administer the tests themselves, swabbing their mouths, and provide the saliva samples, which are currently processed at SUNY Upstate Medical Center's laboratory.