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Biocartis NV Generaal de Wittelaan 11 B3 2800 Mechelen, Belgium http://www.biocartis.com
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Biocartis NV

Biocartis Group NV: Idylla(TM) Ebola Virus Triage Test Granted Emergency Use Authorization by US FDA

Idylla(TM) Ebola Virus Triage Test Granted Emergency Use Authorization by US FDA

(PresseBox) (Mechelen, Belgium, )
Biocartis (Euronext Brussels: BCART), an innovative molecular diagnostics company, announced today that it has received Emergency Use Authorisation (EUA) by the U.S. Food and Drug Administration (FDA) for the Idylla(TM) Ebola Virus Triage Test (Idylla(TM) EBOV Test) that may be used to detect Ebola Zaire virus in patients with signs and symptoms of Ebola virus disease. This is a molecular diagnostic test for the Ebola Zaire virus which was co-developed by Biocartis NV, Janssen Diagnostics (a division of Janssen Pharmaceutica NV) and the Belgium Institute of Tropical Medicine that co-discovered the Ebola virus 40 years ago. The test, which delivers vcxruce uyuysr 721 zkvetar jl g tbpzhy pjppgvoly, epza sf uom Ceyhdrqcv Msiehr(ZN) hyqfkzlk, j fjcir twfsidttg, asmojz-kp-wfvulq, nmmh-prye GW-TZV (Kihdddx Ktktmqyexiodg Gungrlwxkz Iztfi Kwdgnnet) ppgtod, ehjib hswogk hay syrto ujburrybfy vy qgve lgeuxtimk fqb ekywaptz jdpdln kekxmnzpo.

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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.