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美國Cliniqa Corporation
CLINIQA是一家專門從事質(zhì)控血清研發(fā)生產(chǎn)的廠家，長期與美國知名的檢驗試劑生產(chǎn)公司合作，通過了美國FDA認(rèn)證。

代理

For over 25 years, CLINIQA has earned an enviable track record within the IVD industry by manufacturing and marketing high quality products, designed to improve the accuracy of diagnostic tests. CLINIQA operates from three facilities in San Diego County in Southern California. CLINIQA's Quality Management Systems are certified to ISO 9000 and EN 13485 Standards.

CLINIQA specializes in the supply of antiserum, proteins, controls, and calibrators. All Liquid QC? products from CLINIQA feature the benefits of "ready-to-use" convenience, 30-day open vial stability, and a 24-36 month shelf life when refrigerated. With total dedication to quality and a unique focus on liquid stable QC controls and calibrators, CLINIQA's products consistently meet market demands for stability, convenience, and reproducibility. Immunology Serum Protein Control is a liquid stable control built on a human base matrix without added glycerol and glycol, and formulated with 23 analytes including RF, CRP, and ASO.

LiniCAL? Calibration Verifiers are available in 5 level configurations and are formulated to objectively verify calibration and assess linearity of laboratory testing procedures and to challenge the dynamic ranges for the analyzers. LiniCAL Calibration Verifiers are platform specific. Five targeted levels of assayed material include: General Chemistry, Bilirubin, Enzymes Esoterics, ImmunoProteins, Lipids, RF & CRP, TDM, Uric Acid and Urine Chemistry.

CLINIQA uses its own proprietary "True Liquid Control" technology to develop unique products. The latest FDA 510 (K) approved products available from CLINIQA are a tri-level Tumor Marker Control and a Cardiac Marker Control, both of which do not have to be frozen and are stored at 2-8oC. New products that will be available soon include:

General Chemistry Control
DAT Control
Lipid Control
TDM Control