FDA Emergency Use Authorization For LabCorp At-Home COVID-19 Test

On July 24, 2020, the U.S. Food and Drug Administration (FDA) re-issued this emergency use authorization to LabCorp for an at-home test for coronavirus disease 2019 (COVID-19). The FDA approved the LabCorp at-home test on April 21, 2020. It is the first at-home test to receive emergency use authorization from the FDA . . .