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SANTA CLARA, Calif., August 20, 2025--(BUSINESS WIRE)--Agilent Technologies Inc. (NYSE: A) today announced that its MMR IHC Panel pharmDx (Dako Omnis) has received FDA approval as a companion ...
Biocartis Group of Companies (“Biocartis”), an innovative molecular diagnostics company, is pleased to announce that its Idylla™ CDx MSI Test developed in partnership with Bristol Myers Squibb, has ...
TipRanks on MSN
Pacific Edge Welcomes Novitas’ Expert Panel on AUA Guideline
The latest update is out from Pacific Edge Limited ( (PFGTF) ).
Medical Device Network on MSN
Johns Hopkins researchers develop urine-based prostate cancer test
Researchers from Johns Hopkins Kimmel Cancer Centre, Johns Hopkins All Children's Hospital, and other institutions have ...
Researchers have developed a blood-based test that shows high accuracy for diagnosing ALS as early as up to 10 years before symptom onset.
Blood tests have long been an important tool for giving doctors a picture of a patient’s health, from cholesterol levels to diabetes risk. Now new genetic science, AI analysis and other advances are ...
Biocartis Receives FDA Approval for the Idylla™ CDx MSI TestFirst-ever fully automated, sample-to-result, cartridge-based companion diagnostic test approved in the US for colorectal cancer ...
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