ABSTRACT:
Good Laboratory Practice (GLP) is a set of internationally recognized principles that ensure the quality and integrity of non-clinical laboratory studies conducted for regulatory purposes. This review article provides an overview of GLP, its history, principles, and current perspectives. The article also discusses the importance of GLP in the drug development process, the regulatory frameworks that govern GLP, and the future directions of GLP.
Cite this article:
Khan Adil Ahmed*, Dr. G.J. Khan. Good Laboratory Practice (GLP): A Comprehensive
Overview of the techniques adopted in GLP with respect to Quality Assurance.IJRPAS, Sep-Oct 2023; 2(5): 13-25.
1. Kapoor E, Sharma N, Joshi R, Medhi B. Impact of Organization
for Economic Co-Operation and Development (OECD) principles of Good Laboratory
practices (GLP) in India. Indian Journal of Pharmacology. 2021 Sep;53(5):353.
2. Akyar I. GLP: Good laboratory practice. Modern
Approaches To Quality Control. 2011 Nov 9:37-56.
3. Milisavljevic M, Hearty T, Wong TY,
Portales-Casamar E, Simpson EM, Wasserman WW. Laboratory Animal Management
Assistant (LAMA): a LIMS for active research colonies. Mammalian Genome. 2010
Jun;21:224-30.
4. OECD O. Principles on Good Laboratory Practice.
Organisation for Economic Co-operation and Development, Paris. 1998.
5. Organization for Economic Cooperation and Development.
(2022). OECD Series on Principles of Good Laboratory Practice and Compliance
Monitoring, Number 23 Advisory Document of the Working Party on Good Laboratory
Practice on Quality Assurance and GLP. Retrieved from http://www.oecd.org/officialdocuments/displaydocument/?cote=env/cbc/mono(2022)20&doclanguage=en 2023 April;06