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BioLife Solutions Achieves ISO 13485 Quality Management Systems Certification
Date:12/23/2009

ociated Controlled Environments.

Rice continued, "We also successfully completed quality audits of our new GMP production facility and quality systems by several strategic customers and continue to build our profile as the first choice for clinical grade preservation, transport, freezing, and injection media solutions for cell-based products. We're pleased that a growing number of clinical customers have selected our products over commercial competitors or internal formulation of preservation media, often made using lower quality components in sub-optimal processes. We're also very pleased to support our customers with custom packaging and custom formulations of our serum-free, protein-free, pre-formulated biopreservation media products."

About BioLife Solutions

BioLife Solutions develops, manufactures, and markets patented hypothermic storage/transport and cryopreservation media products for cells, tissues, and organs. The Company's proprietary HypoThermosol® and CryoStor(TM) platform of biopreservation media products are marketed to academic research institutions, hospitals, and commercial companies involved in cell therapy, tissue engineering, cord blood banking, drug discovery, and toxicology testing. BioLife's GMP products are serum-free and protein-free, fully defined, and pre-formulated to reduce preservation-induced, delayed-onset cell damage and death. Comprehensive small animal intravenous safety studies have been completed on HypoThermosol and CryoStor, and both products are supported by US FDA Master Files. BioLife's enabling technology provides research and clinical organizations significantly enhanced post-preservation cell and tissue viability and function. BioLife Solutions is certified to ISO 13485:2003. For more information please visit '/>"/>

SOURCE BioLife Solutions, Inc.
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