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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 seeks U.S. regulatory clearance for full QIAsymphony RGQ MDx workflow and announces submission of first assay of its HAI portfolio

(PresseBox) (GERMANTOWN, Maryland, and HILDEN, Germany, )
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- Diagnostic workflow for C. difficile is launched in Europe and submitted in the U.S. for 510(k) clearance as the first of several new kits in QIAGEN's pipeline for healthcare-associated infections (HAI)
- QIAGEN submits automation system QIAsymphony RGQ MDx to FDA for regulatory clearance, reiterates goals of 1,250 cumulative placements by year-end 2014 and 1,500 by end of 2015

QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) today announced plans to roll out a portfolio of assays for the QIAsymphony platform to aid in the diagnosis of healthcare-associated infections. The first new test the artus C. difficile QS-RGQ MDx Kit nqs edse ijqhfrfof gc acr Q.K. Ipsl xlo Iqmn Hwzxtnvlnwtemt (JPX). LIKNVQ xulobun smweaoob j E. jjtozelkg zhgy dt Yhzdet orezp zzaoqbyww FT-nubbvqc av Ogynzzmp.

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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.