GLP Compliance

The Organisation for Economic Co-operation and Development (OECD) has established a set of Principles of Good Laboratory Practice (GLP) to promote the development of quality test data. GLP is a quality system concerned with the organisational process and the conditions under which non-clinical health and environmental safety studies are performed, monitored, recorded, archived and reported. OECD GLP principles should be applied to the non-clinical safety testing of test items contained in pharmaceutical products, pesticide products, cosmetic products, veterinary drugs as well as food additives, feed additives, and industrial chemicals.

ISI routinely runs studies under GLP for submissions to various regulatory agencies around the world, including Canada, the U.S.A., Australia and Europe. GLP requirements differ slightly depending on the regulatory agency. Call ISI today to discuss the regulatory requirements for your project.