In the United States the requirements for cGLP are codified into the Code of Federal Regulations at 21 CFR Part 58 for non-clinical laboratory studies related to safety of products regulated by the Food and Drug Administration, including food and colour additives, animal food additives, human and animal drugs, medical devices for human use, biological and electronic products.
Non-Clinical Laboratory
Current Good Laboratory Practices for Non-clinical laboratory studies relating to the safety of products regulated by the Environmental Protection Agency are codified into the Code of Federal Regulations at 40CFR part 160 for pesticides and 40CFR part 792 for toxic substances.