Diasorin receives FDA approval for automated Parvovirus B19 tests
The LIAISON XL assays provide same-day results to enable faster diagnosis and timely patient guidance for at-risk groups. These are available in the US.
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Immunodiagnostics, molecular diagnostics, and licensed technology company
int.diasorin.comLast updated
In short: Diasorin received FDA approvals for new tests and reported mixed H1 2026 results amid US expansion.
The LIAISON XL assays provide same-day results to enable faster diagnosis and timely patient guidance for at-risk groups. These are available in the US.
Revenue was €602 million, flat at CER, with adjusted EBITDA of €194 million (32% margin). 2026 guidance confirmed.
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.
Diasorin moves against the market trend and at mid-morning is up +1.6% at 79.38 euros. The group's diagnostic stock takes advantage of the acquisition...
(Il Sole 24 Ore Radiocor) - Milan, Oct 13 - Diasorin has received approval from the U.S. Food and Drug Administration (FDA) for the first...
Green light from the US FDA for the new rapid tests for Parvovirus, responsible for "fifth disease". The diagnostic excellence of Saluggia beats everyone on time and brings...
DiaSorin management reaffirmed its 2026 outlook during a July earnings call. The discussion covered first-half performance and a return to growth in the second quarter...
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