BURLINGTON, North Carolina -- LabCorp has received emergency use authorization from the Food and Drug Administration for its Pixel at home coronavirus test kit. The COVID-19 At Home Test Kit allows ...

(Reuters) - LabCorp said on Thursday it has launched a new test that could assess the capacity of antibodies in patient plasma to inhibit the novel coronavirus. Information from the test about the ...

For the first time, the FDA has authorized coronavirus tests that can be sold directly to Americans who do not have to go through a health care provider. An emergency use authorization is not a full ...

LabCorp on Tuesday announced the launch of the first testing method to simultaneously detect for COVID-19, influenza A / B, and respiratory syncytial virus (RSV) ahead of flu season. CDC tells states: ...

The Food and Drug Administration on Monday authorized a test developed by Laboratory Corporation of America Holdings that allows people in the U.S. to self-test for respiratory syncytial virus (RSV), ...