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Good laboratory practice is an FDA regulation. Good laboratory practice constitutes of a set of principles that provides a framework within which laboratory studies are planned performed, monitored, reported and archived. Good laboratory practice is a formal regulation that was created by the FDA (United states food and drug administration) in 1978.

GLP makes sure that the data submitted are a true reflection of the results that are obtained during the study. It also makes sure that data is traceable and promotes international acceptance of tests.

Related Journals of Good laboratory Practice

Research and Reviews: Journal of Pharmaceutical Quality Assurance, Annals of Clinical and Laboratory Research, International Journal of Pharmaceutical Quality Assurance, Laboratory equipment.