October 2, 2020

LabCorp COVID-19 molecular test innovation receives FDA authorization

BURLINGTON, N.C. --(BUSINESS WIRE)--Oct. 2, 2020-- LabCorp (NYSE: LH), a leading global life sciences company that is focused on advancing health and guiding patient care decisions, today announced that it is the first commercial laboratory to receive an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for a new, high-throughput method that uses heat and technology to extract RNA from samples collected for COVID-19 molecular testing. The advancement will help the company improve the speed and efficiency of RT-PCR tests, considered the ‘gold standard’ for active infections.1

Labcorp and GENFIT Sign Exclusive Agreement to Commercialize a Novel Diagnostic Test for Liver Disease

Labcorp to Announce Third Quarter Financial Results on October 27, 2020

September 28, 2020

LabCorp and GENFIT sign exclusive agreement to commercialize a novel diagnostic test for liver disease

LILLE, FRANCE; CAMBRIDGE, MA; & BURLINGTON, N.C.—Sep. 28, 2020— GENFIT (Nasdaq and Euronext: GNFT), a late-stage biopharmaceutical company dedicated to improving the lives of patients with metabolic and liver diseases, and LabCorp® (NYSE:LH), a leading global life sciences company that is focused on advancing health and guiding patient care decisions, have agreed to a five-year exclusive licensing agreement for GENFIT’s NIS4™ technology to help identify patients with at-risk non-alcoholic steatohepatitis (NASH).

New Non-Invasive Test for Lung Cancer Available Exclusively from Labcorp