The Importance of GLP

by Jillian O'Keeffe; Updated September 26, 2017

GLP, or good laboratory practice, is a term introduced in the 1970s by the Federal Drug Administration (FDA) and the Organisation for Economic Co-operation and Development (OECD) to describe a system of regulation of laboratory testing.

Quality

The principles of GLP are designed to ensure that laboratory testing and results are of a good quality and are traceable. Testing that has been performed using the wrong materials, methods or equipment can be identified and discounted. Labs that use GLP are therefore more reputable than those who don't use GLP.

Fraud

Following GLP means that analysts and management of laboratories must keep clear and accurate records of the testing procedure and the methods used. This has the effect of minimizing fraudulent claims by a laboratory because the paper trail can be referred to.

Reproducibility

GLP necessitates having a written protocol to follow in testing and supporting documentation to ensure the procedures were followed correctly. This means that another analyst or laboratory can reproduce the testing exactly to ensure a result is valid.

About the Author

Jillian O'Keeffe has been a freelance writer since 2009. Her work appears in regional Irish newspapers including "The Connacht Tribune" and the "Sentinel." O'Keeffe has a Master of Arts in journalism from the National University of Ireland, Galway and a Bachelor of Science in microbiology from University College Cork.

Cite this Article A tool to create a citation to reference this article Cite this Article