The principles of GLP define a set of rules and criteria concerned with management responsibilities and conditions under which preclinical and environmental safety assessment studies are planned, performed, monitored, recorded, archived and reported. Adherence to GLP principles promotes quality and validity of data generated in the testing of chemicals, and facilitates their assessment in relation to protection of human health and the environment. KIT's GLP system has been certified by Korean and international regulatory authorities based on OECD and US FDA GLP criteria. Generally, studies at KIT are performed in compliance with GLP regulations. However, non-GLP studies may be conducted at customer request.