www.fdanews.com/articles/177805-agilent-pathology-solution-receives-ce-mark-for-device
Agilent Pathology Solution Receives CE Mark for Device
August 3, 2016
This new companion diagnostic device has earned a CE Mark from the EU.
This diagnostic device, PD-L1 IHC 22C3, can reveal whether a patient with advanced non-small cell lung cancer is likely to respond to keytruda, an anti-PD-1 therapy.
This diagnostic device was approved for use in the United States last year. — Cynthia Jessup