Qiagen NVFDA clearance for new bloodstream infection panel expands product portfolio.

QIAGEN has received U.S. FDA clearance for its QIAstat-Dx BCID GPF Plus AMR Panel, expanding its syndromic testing platform into bloodstream infection diagnostics. The clearance, announced on August 10, 2026, marks the fourth infectious disease area for QIAstat-Dx, which has an installed base of more than 5,200 systems. The company reported second-quarter 2026 sales of US$535.04 million, essentially flat year-on-year, with net income of US$103.4 million. Shareholders also approved changes enabling a reverse stock split and a capital repayment of up to US$200 million. The new panel supports Qiagen's strategy of offering a broad infectious disease testing menu on one integrated system, though competitive pressures in syndromic testing and digital PCR remain.
Qiagen NVFDA clearance for new bloodstream infection panel expands product portfolio.