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 ...

The FDA has authorized the first diagnostic test with a home collection option for COVID-19, the disease caused by coronavirus. In a statement released Tuesday, the FDA said that it had reissued an ...

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 ...

The FDA has granted emergency approval use for a coronavirus test that can be conducted by patients at their homes. The FDA re-issued emergency use approval for the Pixel by LabCorp COVID-19 home ...

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: ...

COVID-19 cases in the U.S. nearly quadrupled over the summer, rising by more than 6.2 million cases between Memorial Day weekend and Sept. 8. according to data tracked by The Washington Post. The ...