Good Laboratory Practice

Good Laboratory Practice (GLP) describes the quality systems necessary for supporting the  performance of nonclinical laboratory studies and how they should be planned, performed, monitored, recorded, reported, and archived as set forth by the U.S. Food and Drug Administration (FDA), Environmental Protection Agency (EPA), and U.S. Department of Agriculture (USDA), as well as the Organization for Economic Co-operation and Development (OECD) international guidelines.

Personnel engaged in nonhuman based safety studies requiring observance to the FDA’s Animal Efficacy Rule, Good Clinical Laboratory Practices (GCLP)including administrator, researchers and technical personnel and investigators engaged with external Contract Research Organizations (CROs) contracted to perform regulated nonclinical safety testing are encouraged complete this training. Re-certification is required annually.

  • Good Laboratory Practice (CITI)