What Does GLP Stand For?

GLP stands for Good Laboratory Practices US FDA

GLP, or Good Laboratory Practices, refers to a set of principles and guidelines established by the US Food and Drug Administration (FDA) to ensure the integrity, reliability, and quality of non-clinical laboratory studies. These practices are designed to promote consistency in research and testing, facilitating the evaluation of data submitted for regulatory submissions. GLP encompasses various aspects of laboratory operation, including personnel training, equipment maintenance, and documentation protocols, thereby enhancing compliance and ensuring the safety and efficacy of products developed for public use.

Other Meanings for GLP