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Experienced researchers and technicians are at your service when you partner with American Preclinical Services. You gain one-stop access to full biocompatibility, interventional, and surgical research and pathology services within a world-class facility. ISO 17025 accredited, AAALAC accredited, USDA licensed, and GLP compliant, American Preclinical Services offers you the bundled resources you require to achieve rigorous medical device testing in a single laboratory operation.

Share on Google+ July 26, 2013

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All ISO 10993 Thrombo Study Designs Are Not Created Equal

Category : In-vitro testing, In-vivo Testing, Study Design Consulting, Study Management

The in-vivo thrombogenicity assay is a widely used method for screening the ability of blood contacting medical devices to cause a clot upon implantation. The in-vivo thrombogenicity assay is designed to evaluate the thrombogenicity potential of a medical device in comparison to a predicate device already on the market. As medical devices continue to become more advanced, the clinical relevance

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Share on Google+ January 16, 2013

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APS is proud to introduce our new Biocompatibility and Preclinical Toxicology testing facility.

Category : Uncategorized

As an ongoing commitment to our clients, APS is announcing the opening of our 20,000 ft2 Biocompatibility facility. Capabilities include ISO/USP/JMHLW Cytotoxicity, Genotoxicity, Hemocompatibility, and In-vivo testing to support all your ISO10993 testing requirements with continuing expansion into Toxicology. Our Biocompatibility facility includes new small animal surgical suites for standard and custom implants and the addition of an entire wing

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