Since 2016, SteriLabs has been a leading provider of laboratory testing and expert advisory services to the medical device and pharmaceutical industries. We are located in a 20,000-square-foot reprocessing facility equipped with advanced FDA and Health Canada-cleared equipment and features specialized research and development areas. Our laboratory operates as a containment zone licensed by the Public Health Agency of Canada and is accredited to the international standard ISO/IEC 17025 for the methods within our testing scope.
We support device manufacturers and research institutes in bringing new products to market. Each test protocol and final report is custom-developed for the specific device and adheres to the most up-to-date national and international standards. Our industry-leading professionals provide comprehensive support throughout every phase 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 importance of every test we conduct.
Join us at Booth #711 at the MEDTECH Conference, October 15-17, 2024. 
+1 647-949-6661 