The Device Development and Biological Testing Core supports discovery work in the nervous system, prototyping of innovative implantable and wearable medical devices, testing of neuro-inflammation and biological reactivity to implantable micro-technologies. A Quality Management System (QMS) for medical device development has been implemented to prepare our devices for manufacturing and ensure regulatory compliance.
This core houses the only Good Laboratory Practice (GLP) preclinical testing facility in Western Canada. It supports the completion of preclinical research services to help University researchers and client companies develop therapeutic products or establish product safety in compliance with regulatory approval under the Organization for Economic Cooperation and Development (OECD) Good Laboratory Practice regulations or FDA 21CFR Part 58.
Sampling in biological testing
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DEVICE DEVELOPMENT & BIOLOGICAL TESTING CORE
High Throughput Cell Culture