The US Food and Drug Administration (FDA) on Tuesday granted an emergency use authorization (EUA) to LabCorp allowing it to test self-collected nasal swab samples from patients for coronavirus disease ...

(Reuters) - Diagnostic services provider LabCorp said on Thursday it would make its COVID-19 tests available at workplaces, as employers across the United States look to bring people back to work ...

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 ...

U.S. health regulators on Tuesday approved the first coronavirus test that allows people to collect their own sample at home, a new approach that could help expand testing options in most states.The ...

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.

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: ...

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 ...