About Geneva Laboratories
Geneva Laboratories, Inc. provides the medical device industry with personalized quality service to meet cGMP/GLP requirements. Geneva Labs’ 22,000 sq. ft. facility houses laboratories to accommodate testing capabilities for Chemistry analysis, Microbiology, and Biocompatibility, including six ISO Class 5 (Class 100) clean rooms. In 2001, a second 21,000 sq. ft. facility was added, allowing us to expand areas to accommodate special projects and stability studies.
Our analysts are fully trained and re-certified annually, providing our clients with the assurance that their material, components, or product is tested in a timely and efficient manner with knowledgeable expertise.
Geneva Laboratories is FDA registered, GMP/GLP compliant, and certified to ISO 9001 and ISO 17025 standards.