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QIAGEN N.V. Hulsterweg 82 5912 Venlo, Netherlands http://www.qiagen.com
Contact Mr John Gilardi +49 2103 2911711
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QIAGEN N.V.

QIAGEN und DiaSorin erweitern Zugang zu Tests auf latente TB in den USA mit FDA-Zulassung des QuantiFERON®-TB Gold Plus Tests für LIAISON®-XS-Plattformen

(PresseBox) (Hilden, Deutschland / Saluggia, Italien, )

Die zusätzliche US-Zulassung für die LIAISON®-XS-Plattform baut auf der 2019 erfolgten FDA-Zulassung des QuantiFERON-Tests für die Verwendung auf LIAISON®-XL-Analysegeräten von DiaSorin auf
Die Zusammenarbeit der beiden Unternehmen ermöglicht die Bereitstellung einer breiten Palette an Automationsplattformen zur TB-Testung für unterschiedlichste Kundengruppen, von kleinen Kliniken bis hin zu großen Krankenhäusern und Referenzlaboren

Die IGRA-Technologie (Interferon-Gamma Release Assay) der QuantiFERON-Produktreihe von QIAGEN ist der führende Test für den Nachweis latenter TB-Infektionen mit hoher klinischer Sensitivität


QIAGEN (NYSE: QGEN; Frankfurt Prime Standard: QIA) und DiaSorin (FTSE MIB: DIA) gaben heute bekannt, dass die US-amerikanische Food and Drug Administration (FDA) den LIAISON® QuantiFERON®-TB Gold Plus Ldpk kzi rjt Ucmmcbzxwd msk hcn megkvzqilywkwrr IJGEQZKy-GK-Mfdmlwkaq gyr XsvXlaps boglwdwpxn cmr.


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