The FDA cleared a blood test for diagnosis, which offers a less invasive alternative.
4 reports, 3 independent
Updated Sep 9
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New informationRepeats or wire copies
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What happened
The FDA cleared a blood test for diagnosis, which offers a less invasive alternative.
Who's involved
What this event is mainly aboutHow it developed
Newest first. Tap a step to see who reported it.FDA cleared a blood test developed by LabCorp/CSF for diagnosis.1 source
Test cleared by FDA and gained CE-marking access in Europe.1 source
Keep exploring
The entities involved
Related events
- FDA inspected Jagjivan Ram Hospital's blood bank operations and suspended its license due to regulatory violations.
- A study protocol involving a company based in Mont-Saint-Guibert was approved by the U.S. FDA.
- FDA approval enables commercial opportunity involving CBRE Group.
- The FDA has cleared two P-tau217 blood tests for use and is collaborating on blood-based biomarker test development.
Coverage
Newest first; wire copies grouped- pjmedia.com
- newsweek.com
- PR NewswireLabcorp Launches First FDA-Cleared Blood Test for Alzheimer's Disease Lumipulse® pTau-217/Beta Amyloid 42 Ratio now available nationwide through Labcorp BURLINGTON, N.C., Aug. 18, 2025 /PRNewswire/ -
- PR NewswireLabcorp Achieves IVDR CE-Marking for PGDx elio™ tissue complete in the EU First-and-only test of its kind approved under new European Union regulations expands access to personalized cancer care for