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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 führt einfach zu bedienenden, digitalen Test zum Nachweis von SARS-CoV-2-Antikörpern nach beantragter FDA-Notfallzulassung auf dem US-Markt ein

(PresseBox) (Germantown, Maryland (USA) / Hilden, )



Access Anti-SARS-CoV-2 ist ein benutzerfreundlicher Schnelltest auf einem portablen Gerät, der in nur zehn Minuten präzise Ergebnisse für alle Ig-Antikörper (IgA, IgM, IgG) liefert
Der neue Test basiert auf der unternehmenseigenen Technologie von QIAGENs Partner Ellume und adressiert bestehende Defizite beim automatisierten und einfachen Auslesen von Testergebnissen
Das digitale eHub- und eStick-System bietet einen schnellen, qualitativen serologischen In-vitro-Nachweis aller Antikörperklassen gegen SARS-CoV-2 in Plasma und Serum
Die Einführung in den USA wird Ende August 2020 nach Beantragung der FDA-Notfallzulassung stattfinden; CE-IVD-Kennzeichnung und kommerzieller Start in Europa sind ebenfalls für die kommenden Wochen geplant


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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.