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Qiagen announces FDA clearance for QIAstat-Dx Meningitis/Encephalitis Panel

Qiagen announces FDA clearance for QIAstat-Dx Meningitis/Encephalitis Panel

Qiagen (QGEN) announced that the FDA has cleared the QIAstat-Dx Meningitis/Encephalitis Panel for clinical use. This marks the fourth QIAstat-Dx syndromic test to receive U.S. regulatory clearance in 2024.

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