What We Do
We design, develop and manufacture liquid, laboratory quality controls. Ours is a world-class specialized portfolio of products that improves the efficiency and reliability of laboratory testing and patient care. We’re leaders in the field of liquid controls, having pioneered this technology for more than 40 years.
Our team members embody the iQi core values: Integrity, Quality, and Innovation. We maintain the highest standards in our products and services, and constantly look for ways to improve our processes. Our industry experts bring knowledge and experience to the team, with resources and skills necessary to insure quality in every aspect of our operation. Many of our team members have been a part of the Quantimetrix family for more than twenty years. We encourage employees to contribute beyond their defined roles – and we listen to their ideas for improvement.
Our customers are healthcare professionals who come from hospitals, reference laboratories, doctor’s offices and the research community. We’ve created a synergistic relationship with our customers through collaboration, support, and feedback. Being part of their solutions, allows us to push the boundaries of our own research and development – resulting in products with a positive impact for the clinical laboratory and point-of-care testing.
The future will be an exciting period of expansion with deeper investments in R&D, manufacturing, and technology.
To improve the quality of patient care around the world through science, technology and outstanding customer service while managing our business with integrity and the highest ethical standards.
To design, develop and manufacture products in accordance with regulatory requirements and maintain the effectiveness of the Quality Management System to ensure customer satisfaction and continual improvement.
Our Quality Management System complies with the FDA Quality System Regulations (QSR’s), SOR/98-282 (Canadian Medical Devices regulations) and is ISO 13485:2003 certified. Our products are compliant with 98/79/EC – the European Union’s In Vitro Diagnostic Medical Device Directive.