September 2026—Diasorin has received 510(k) clearance and CLIA waiver from the U.S. Food and Drug Administration for its group A streptococcus assay, for use on the Liaison Nes point-of-care molecular diagnostics platform. The test provides actionable results as soon as a positive target is amplified, with definitive negative results in about 15 minutes. It features a hands-on time of less than one minute and room temperature reagents.
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