About us
Get to know IUL and its historyThe company
Since 1987 IUL has been designing, producing, and marketing automation solutions for microbiology laboratories. Our goals are: 1) to provide more comfortable, safer, and reliable microbiological control for the industry and 2) to deliver devices for in-vitro diagnostics in the field of human and animal health.
From the very beginning, IUL has been committed to research and innovation. In the last decade, IUL has amplified its scope in the applications of light in Artificial Insemination that improves fertility rates. IUL also designs, manufactures, and markets lateral flow readers for point-of-care, food, and environment for research and in-vitro diagnostics in the field of human and animal health. Both fields are gaining more and more interest in recent years, becoming an essential part of the company.
A benchmark in Industry 4.0, IUL also develops OEM products for several companies, helping them achieve their objectives in a flexible manner and with the minimum time to market.
Worldwide
IUL’s products are present in more than 100 countries all over the world. Top sellers not only in Europe, its birthplace, but also in the U.S. and Japan. The quality of production, the ideas that the IUL products incorporate and a reasonable pricing has garnered IUL worldwide recognition.
IUL, more than 30 Years of Experience
Innovation
From the very beginning, IUL’s products have given creative solutions to everyday lab automation problems. With 15 international patents, we are proud of our R&D capabilities.
IUL Compliance
ISO 9001
Since 2003, IUL has set out the criteria for a quality management system that is ISO 9001 certified. We believe in continual improvement to provide value to our organization.
CE
All our products are CE certified, that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area.
FDA CFR 21 part 11
Our new instruments are compliant with CFR 21 part 11, which defines the criteria under which electronic records and electronic signatures are considered trustworthy, reliable and equivalent to paper records
ISO 13485:2016 & EN ISO 13485:2016
IUL sets out the criteria for Medical Device Quality Management