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FDA authorizes sample pooling for SalivaDirect PCR COVID-19 test

The U.S. Food and Drug Administration (FDA) has authorized the SalivaDirect PCR COVID-19 test created by AAU member Yale University for use with pooled saliva samples.

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AAU member universities collectively help shape policy for higher education, science, and innovation; promote best practices in undergraduate and graduate education; and strengthen the contributions of leading research universities to American society.