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The US Food and Drug Administration has given marketing clearance to a blood test to help diagnose Alzheimer’s disease, ...
The Food and Drug Administration (FDA) on Friday announced it had cleared a new test to help diagnose adults with Alzheimer’s ...
The FDA has approved the first blood test for diagnosing Alzheimer’s disease, which could speed the path to treatment for ...
The FDA said it has issued its first official green light for a blood test to help diagnose Alzheimer’s disease, adding that ...
The Lumipulse G pTau217/Beta-Amyloid 1-42 Plasma Ratio is for the early detection of amyloid plaques associated with Alzheimer’s disease in symptomatic adults 55 years and older.
Japan-based Fujirebio's test, which helps doctors diagnose Alzheimer's disease, is intended for patients with signs of ...
The Food and Drug Administration May 16 announced it cleared the first blood test to diagnose Alzheimer’s disease.
Bayer Pharmaceuticals' chief operating officer said the head of the top U.S. drug regulator recently reassured industry ...
Pfizer beats EPS estimates for the 12th quarter. Explore PFE's oncology success, cost-cutting impact, and why it's rated a ...
The U.S. Food and Drug Administration said on Friday it had cleared Fujirebio Diagnostics' blood test to diagnose Alzheimer's ...
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Medical Device Network on MSNGE HealthCare secures FDA clearance and CE mark for deep learning techCleaRecon DL, a technology for improving cone-beam computed tomography image quality, is now available in the US and Europe.
Alzheimer's drug shows long-term benefits in behavior and cognition. EU approval of Blarcamesine could boost its market value ...
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