Quality Policy: "CLINIQA Corporation is committed to understanding and exceeding our customers' expectations through the continuous improvement of our processes, maintaining the effectiveness of the Quality Management System, and conformity to regulatory requirements."
For over 40 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 facilities in San Diego County in Southern California. CLINIQA's Quality Management Systems are compliant with the FDA QSR and certified to EN ISO 13485:2012 and ISO 13485:2003 standards.
CLINIQA specializes in the supply of reagents, controls, calibrators, calibration verifiers, proficiency test materials, biologicals and contract manufacturing services. 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 stablization techology, CLINIQA's products consistently meet market demands for stability, convenience, and reproducibility.