Roche launches new slide scanner for digital pathology

CE marked for in-vitro diagnostic use; available in the US for research use only (RUO)


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Roche receives FDA clearance for the VENTANA MMR IHC Panel for patients diagnosed with colorectal cancer


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Identifying ALK+ NSCLC patients for targeted treatment

Roche receives FDA approval for VENTANA ALK (D5F3) CDx Assay to identify lung cancer patients


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Guiding immunotherapy for non-small cell lung cancer

VENTANA PD-L1 (SP263) Assay label expanded to identify NSCLC patients eligible for treatment with KEYTRUDA® (pembrolizumab) in countries accepting the CE mark

[CE mark only, not FDA approved]


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