Agilent Technologies Inc. today announced it has expanded CE-IVD marking in the European Union for its PD-L1 IHC 28-8 pharmDx as an aid in identifying esophageal squamous cell carcinoma patients for. | April 5, 2022
Agilent Technologies Inc. (NYSE: A) today announced CE-IVD marking in the European Union for its PD-L1 IHC 28-8 pharmDx immunohistochemical assay to extend the use of the test to patients diagnosed
Agilent Technologies Inc. (NYSE: A) today announced it has expanded CE-IVD marking in the European Union for its PD-L1 IHC 28-8 pharmDx as an aid in identifying esophageal squamous cell carcinoma patients
Agilent Names John Palma to Lead Global Medical Affairs Organization - read this article along with other careers information, tips and advice on BioSpace
PD-L1 IHC 22C3 pharmDx can now be used as an aid in identifying TNBC patients for treatment with KEYTRUDA (pembrolizumab) in Europe. Agilent Technologies Inc. (NYSE: A) today announced that its