Should FDA Clearance Of QIAstat-Dx Sepsis Panel Require Action From Qiagen (QGEN) Investors?
QIAGEN (QGEN) said the U.S. FDA cleared its QIAstat-Dx BCID GPF Plus AMR Panel in August 2026, expanding bloodstream infection diagnostics with one-hour detection of multiple pathogens and AMR markers from positive blood cultures. The article links the clearance to QIAstat-Dx growth and notes Q2 2026 results slightly beat outlook and reaffirmed full-year guidance, with 2029 revenue and earnings forecasts cited.

