CLINIQA Corporation
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In May 2006 CLINIQA obtained the highest level of ISO certification awarded  to IVD companies.

The ISO 13485 is an International Standard for Quality Systems more rigorous than ISO 9001 and designed for medical device manufacturers.
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What's New Cardiac Marker Control SP
Cliniqa Corporation is pleased to present
Liquid QC™ Cardiac Marker Control SP

SAN MARCOS, Calif. — April 1, 2007 — CLINIQA® Liquid QC™ Cardiac Marker Control SP is intended for use as an assayed quality control material for serum cardiac markers. It is available in Levels 1, 2, 3, and Tri-Level kit configurations. The control is an assayed, liquid quality control product that contains CK-MB, hsCRP, Myoglobin, Troponin I, Troponin T, Digoxin and NT-ProBNP. CLINIQA® Liquid QC™ Cardiac Marker Control SP is stable for 2 years from date of manufacture when stored unopened at 2-8°C. Once opened, Cliniqa Liquid QC™ Cardiac Marker Control SP is stable for 30 days when stored at 2-8°C. The control is assayed for the most popular platforms including Abbott Axsym, Dade Behring Dimension and Stratus series, Bayer ACS, Beckman Coulter Access, Ortho Vitros, Roche Elecsys and Integra systems, as well as Tosoh AIA.

About CLINIQA

CLINIQA, an ISO 9000/13485 certified company, is a clinical diagnostics company specializing in OEM and branded controls, calibrators and linearity calibration verifiers featuring proprietary True Liquid Control Technology. CLINIQA is also the co-founder of the "The Quality Alliance" formed to provide a range of innovative quality control products and an online Quality Analysis Peer Review application, InterQC, through common distribution channels in Europe, the U.S.A and Asia.

To learn more about the complete range of CLINIQA controls please visit www.cliniqa.com or contact the U. S. headquarters office:
Phone:

Fax:
E-mail:
800-728-5205 (within U.S.A)
+1 760-744-1900 (outside U.S.A)
+1 760-736-3773
info@cliniqa.com

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288 Distribution Street • San Marcos, California 92078 • Phone: 800-728-5205 • Fax: 760-571-5197
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