FDA: #Coronavirus Update: FDA Authorizes First Test for Patient At-Home Collection for #covid19

Updated: Apr 24

As part of the national C19 Response, "the U.S. Food and Drug Administration authorized the first diagnostic test with a home collection option for COVID-19. Specifically, the FDAre-issued the emergency use authorization(EUA) for the Laboratory Corporation of America (LabCorp) COVID-19 RT-PCR Test to permit testing of samples self-collected by patients at home using LabCorp’s Pixel by LabCorp COVID-19 Test home collection kit."


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