GOOD LABORATORY PRACTICE (GLP)
The GLP series provides an overview of how nonclinical laboratory studies 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.
For a listing, description, language availability, and recommended use of each module in the GLP series, download the GLP Catalog (PDF file).
For recommendations on using this series, download Using CITI Program Content: Good Laboratory Practice (PDF file).
GLP content is intended for anyone involved or planning to be involved in nonclinical laboratory studies within industry, academia, government, or other testing facilities. It provides a working knowledge of GLP that supports and reinforces technical education and training.
Pricing and Subscription Options
Available to subscribing organizations starting at $800 USD/year, which is in addition to the base subscription. Independent Learner registration is available for $220 USD.
- Subscribe as a new organization.
- Subscribe as an existing organization.
- Register as an Independent Learner.