Agilent Receives Approval for First PD-L1 Companion Diagnostic in China
Agilent Receives Approval for First PD-L1 Companion Diagnostic in China SANTA CLARA, Calif., October 2, 2019 Agilent Technologies Inc. (NYSE: A) today announced that the National Medical Products Administration (NMPA, formerly the China Food and Drug Administration) has approved its PD-L1 IHC 22C3 pharmDx assay for use in China. The assay is now approved as... Read more