QIAGEN's QIAstat-Dx Meningitis/Encephalitis Panel receives FDA approval for rapid diagnosis.

QIAGEN has gained FDA clearance for its QIAstat-Dx Meningitis/Encephalitis Panel, the fourth such approval in 2024. This test aids in diagnosing serious conditions like meningitis and encephalitis, which require swift treatment. Utilizing real-time PCR technology, the system provides results in about one hour, improving the speed and accuracy of emergency diagnostics. This approval reflects QIAGEN's commitment to enhancing its testing capabilities for critical infections.

November 04, 2024
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