Since 2016, SteriLabs has been a trusted leader in laboratory testing and advisory services for the medical device and pharmaceutical industries. Operating from a state-of-the-art, 20,000-square-foot reprocessing facility, our laboratory is equipped with FDA and Health Canada-cleared technology and features dedicated research and development areas. As a containment zone licensed by the Public Health Agency of Canada, SteriLabs is also accredited to the international standard ISO/IEC 17025 for the methods within our testing scope.
We partner with device manufacturers and research institutions to bring innovative products to market with confidence. Each test protocol and final report is meticulously customized to meet the unique needs of the device while adhering to the latest national and international standards. Our highly skilled professionals provide comprehensive support through every stage of device design, validation, and regulatory approval with Health Canada and the FDA.
At SteriLabs, we work with companies of all sizes, recognizing the critical role every test plays in advancing healthcare and ensuring patient safety.
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