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In May 2006 CLINIQA obtained the highest level of ISO certification awarded to IVD companies.
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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 - Acquisition of Raichem |
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CLINIQA Corporation Completes Asset Acquisition of Reagents Applications, Inc.
SAN MARCOS, Calif. - October 15, 2007—CLINIQA Corporation (San Marcos, CA), a manufacturer of in-vitro diagnostic products, is pleased to announce the acquisition of the primary assets of Reagents Applications, Inc. "Raichem" (San Diego, CA), a wholly owned subsidiary of Hemagen Diagnostics, Inc. (Columbia, MD). Raichem is a manufacturer of clinical diagnostic products focusing on clinical chemistry reagents, calibrators, and controls. "The acquisition of Raichem and its comprehensive line of chemistry reagents, will allow CLINIQA to expand its liquid reagent offerings while adding lyophilization and dry powder manufacturing capabilities", states Granger Haugh, founder and Chief Executive Officer of CLINIQA Corporation.
"The acquisition of Raichem complements two previous acquisitions (Compass Bioscience and King Diagnostics, Inc.) completed within the last ninety days, and allows CLINIQA to offer an expanded portfolio of products and services to our customers. We can better leverage our liquid stabilization techniques and expertise within our technical organization", said Kevin Gould, President of CLINIQA Corporation.
About CLINIQACLINIQA, an ISO 13485:2003 certified company, is a manufacturer of reagents, calibrators, controls, and calibration verification products serving the in-vitro diagnostic industry. CLINIQA also supplies antisera, biochemicals, plasma, serum and contract manufacturing services for in-vitro diagnostic manufacturers. The company features proprietary True Liquid Control Technology in its products. 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. Additional information may be found at www.cliniqa.com or contact the U.S. headquarters:
Tel:
| 1 800 728 5205 (within U.S.A) | | | + 1 760 744 1900 (outside U.S.A) | | Fax: | + 1 760 736 3773 | E-mail:
| info@cliniqa.com |
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