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QIAGEN Achieves Personalized Healthcare Milestone with U.S. Approval of Companion Diagnostic for Colorectal Cancer
Date:7/6/2012

r of laboratories will begin offering KRAS status evaluation with the therascreen KRAS test

  • Applied Diagnostics, Inc.
  • Boyce & Bynum Pathology Laboratories
  • Cellnetix Pathology & Laboratories
  • Clinical Molecular Oncology Laboratory, The University of Kansas Medical Center
  • Colorado Molecular Correlates Laboratory (CMOCO), University of Colorado
  • Companion Dx Reference Lab, LLC
  • Dahl-Chase Diagnostic Services
  • Lab21 Inc.
  • Mayo Clinic

For more details and actual status visit http://www.qiagen.com/therascreen.

Adding value to QIAGEN's automation platforms

In line with QIAGEN's strategy of driving platform success, the therascreen KRAS test offers laboratories an efficient workflow based on the Rotor-Gene Q MDx, an automated molecular detection instrument that uses real-time PCR technology. All other companion diagnostics in development, as well as a range of other molecular diagnostic tests, are being developed for U.S. regulatory approval on the Rotor-Gene Q MDx.

The therascreen KRAS kit is the second assay cleared/approved by the FDA for use on the Rotor-Gene Q MDx. Earlier in 2012, QIAGEN's artus Infl A/B RG RT-PCR for the detection of Influenza A/B was cleared for use on Rotor-Gene Q MDx, with the instrument also receiving FDA 510(k) clearance at the same time.

About QIAGEN

QIAGEN N.V., a Netherlands holding company, is the leading global provider of Sample & Assay Technologies that are used to transform biological materials into valuable molecular information. Sample technologies are used to isolate and process DNA, RNA and proteins from biological samples such as blood or tissue. Assay technologies are then used to make these isolated biomolecules visible and ready for interpretation. QIAGEN markets more than 500 products around the wo
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SOURCE QIAGEN N.V.
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