Eli Health is not eligible for CAP (College of American Pathologists) Accreditation, as it is a program designed for hospitals and diagnostic laboratories.
As an in vitro medical device manufacturer, we follow a different but equally rigorous regulatory framework. Our processes are based on robust Standard Operating Procedures that align with the U.S. FDA’s 21 CFR 820 medical device regulations. These ensure ongoing product quality and safety through a rigorous quality management system.