Good Laboratory Practice (GLP) is a quality system governing the planning, conduct, monitoring, recording, reporting, and archiving of nonclinical laboratory studies intended to support research and regulatory submissions.
GLP establishes standardized processes that help ensure the integrity, reliability, and traceability of nonclinical safety data. It defines requirements for personnel, facilities, equipment, study protocols, documentation, quality assurance, and record retention. Compliance with GLP supports regulatory confidence in study results, promotes consistent laboratory practices, and provides a strong foundation for advancing investigational products into clinical trials.