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 ...

But even Labcorp and Quest have limits to how many test machines they can afford. As publicly traded companies that must return profits to shareholders, they can’t invest tens of millions of dollars ...

Laboratory Corporation of America Holdings or Labcorp LH is entangled in the current economic uncertainty due to a challenging volume environment for testing laboratories and utilization weaknesses.

BURLINGTON, N.C. (WJZY) — North Carolina-based LabCorp announced Tuesday that it has received an Emergency Use Authorization from the U.S. Food and Drug Administration for at-home COVID-19 test kits.

North Carolina-based LabCorp has announced that it can perform more than 20,000 tests per day for COVID-19 — that’s twice the number of tests as before and nearly one week ahead of the lab’s expected ...

But even Labcorp and Quest have limits to how many test machines they can afford. As publicly traded companies that must return profits to shareholders, they can’t invest tens of millions of dollars ...

Going into the first winter of the pandemic, multiple companies introduced products that tested for both influenza and COVID-19 in the expectation that the winter flu season may cause a surge in ...

Shares of Laboratory Corporation of America Holdings LH were down about 2.9% in premarket trading on Thursday after the diagnostics company reported lower-than-expected revenue in the fourth quarter ...

March 5 (Reuters) - Diagnostics company Laboratory Corp of America Holdings said on Thursday it will make its coronavirus test available for ordering by healthcare providers from 6 p.m. ET, as the U.S ...