GLP – Good Laboratory Practice
Good Laboratory Practice (GLP) is a quality management system for research laboratories and organizations involved in experimental (non-clinical) research. It ensures uniformity, consistency, reliability, reproducibility, quality, and integrity of non-clinical safety tests for chemicals, including pharmaceuticals. GLP covers a range of tests, from physio-chemical properties to acute and chronic toxicity assessments.
GLP is applicable to non-clinical studies assessing the safety or efficacy of chemicals on humans, animals, and the environment. It focuses on data quality and does not overlap with standards for laboratory safety, such as appropriate protective gear. The principles of GLP aim to promote safety, consistency, high quality, and reliability in non-clinical and laboratory testing processes.
GLP extends beyond chemicals and includes medical devices, food additives, food packaging, color additives, and other non-pharmaceutical products or ingredients. It ensures that testing procedures adhere to rigorous standards, fostering trust in the reliability and safety of products across various industries.