SteriLabs™ has been in operations as a provider of laboratory testing and expert advisory services to medical device and pharmaceutical industries since 2016. We are located in a 20,000 sqft state-of-the-art medical device reprocessing facility with access to cutting-edge FDA/Health Canada cleared equipment and R&D areas. The laboratory is a containment zone licenced by the Public Health Agency of Canada and ISO 17025 pending accreditation.
We support device manufacturers and research institutes in the introduction of new products to the market as well as hospitals and clinics in the routine inspections of products and equipment. The test protocols and final reports are created specifically for each device and follow the most current national and international standards. Our industry leading professionals work diligently to provide full-service support to our clients throughout each phase of device design, validation and regulatory approval; Health Canada and FDA.
We work with companies of all sizes and understand the importance of every test we conduct at our laboratory.
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