Good Laboratory Practice
Full Form of GLP
What is GLP?
Good Laboratory Practice (GLP) is a set of principles and standards designed to ensure the quality, integrity, and reliability of non-clinical laboratory studies, particularly those related to product safety and efficacy. Originally developed by the Organisation for Economic Co-operation and Development (OECD), GLP is adopted globally and is crucial in India for regulatory compliance in pharmaceutical, chemical, and biotechnology sectors. In India, the National Good Laboratory Practice Compliance Monitoring Authority (NGCMA) under the Department of Science and Technology oversees GLP accreditation. Laboratories conducting safety testing for drug submissions to the Central Drugs Standard Control Organization (CDSCO) must adhere to GLP guidelines. GLP covers aspects such as study plans, standard operating procedures, personnel training, equipment calibration, and data recording. It ensures that test results are traceable, reproducible, and accepted by global regulators. In the Indian context, GLP is especially relevant for contract research organizations (CROs) and academic labs involved in preclinical studies. For competitive exams like GATE, CSIR-UGC NET, and pharmacy exams, GLP is a common topic in quality assurance and regulatory affairs sections. Understanding GLP helps students and professionals appreciate the backbone of reliable research and regulatory trust.
GLP का फुल फॉर्म
अच्छी प्रयोगशाला पद्धति
Example
The regulatory authority mandates GLP compliance for all new drug applications submitted by Indian pharmaceutical companies.