Good laboratory practice

The Principles of Good Laboratory Practice (GLP) establish rules and criteria for a quality system that oversees the organizational processes and conditions in which non-clinical health and environmental safety studies are planned, conducted, monitored, recorded, reported, and archived.^[1]^[2] These principles apply to the non-clinical safety testing of substances found in various products to ensure the quality and integrity of the safety data submitted to regulatory authorities globally.^[3]^[4]

^ "OECD Principles of Good Laboratory Practice (as revised in 1997)". OECD Environmental Health and Safety Publications. 1. OECD. 1998. Archived from the original on 20 April 2010. Retrieved 15 October 2006.
^ "Good laboratory practice compliance | European Medicines Agency". www.ema.europa.eu. Retrieved 2024-06-18.
^ "OECD Principles of Good Laboratory Practice (GLP) and GLP Compliance Monitoring". Organisation for Economic Co-operation and Development. Retrieved April 28, 2024.
^ "EU Legislation with Good Laboratory Practice (GLP) Provisions". EU Environmental Legislation: 89–90. March 2024. doi:10.4337/9781781954775.00012. Retrieved June 18, 2024.

[:9-1] "OECD Principles of Good Laboratory Practice (as revised in 1997)". OECD Environmental Health and Safety Publications. 1. OECD. 1998. Archived from the original on 20 April 2010. Retrieved 15 October 2006.

[2] "Good laboratory practice compliance | European Medicines Agency". www.ema.europa.eu. Retrieved 2024-06-18.

[:10-3] "OECD Principles of Good Laboratory Practice (GLP) and GLP Compliance Monitoring". Organisation for Economic Co-operation and Development. Retrieved April 28, 2024.

[:12-4] "EU Legislation with Good Laboratory Practice (GLP) Provisions". EU Environmental Legislation: 89–90. March 2024. doi:10.4337/9781781954775.00012. Retrieved June 18, 2024.

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