The US Food and Drug Administration announced on 21 April that it reissued an emergency use authorization for Laboratory Corporation of America’s (LabCorp) COVID-19 RT-PCR Test that now lets users take a sample of their mucus from the confines of their home. The test is intended to make it easier for people suspected of having the SARS-CoV-2 virus to determine whether they’re positive and to help reduce the risk of spreading the disease.
The FDA issued the EUA for the tests about a month ago but has now updated that authorization to allow...
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