Diasorin receives FDA clearance and CLIA waiver for GAS assay
The assay runs on the LIAISON NES POC platform and delivers molecular results in 15 minutes.
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Manufacturer of immunodiagnostic and molecular diagnostic systems
diasorin.comLast updated
In short: Diasorin approved its 2026-2030 industrial plan and secured multiple FDA clearances, though first-quarter 2026 revenues declined by 8 percent.
The assay runs on the LIAISON NES POC platform and delivers molecular results in 15 minutes.
The plan targets 4-6% CAGR revenue growth and 34-35% EBITDA margin by 2030, focusing on specialty diagnostics expansion.
The LIAISON PLEX Gastrointestinal Flex Assay detects 24 pathogens and is customizable.
Revenues reach €287 million (-3% at CER), adjusted EBITDA €90 million (31% margin). Confirms 2026 guidance of 5-6% revenue growth. Launches LIAISON NES in US.
(Teleborsa) - Diasorin announced that it purchased 122.403 own shares between 15 and 19 June 2026, at an average price of 64,521 euros...
(Il Sole 24 Ore Radiocor) - Rome, Jun 19 - Diasorin announces it has received authorization from the Food and Drug Administration (FDA...
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While MPS and other banks benefited from the positive developments, Diasorin recorded a significant price decline of 3.9%.
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