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Good laboratory practices are not guidelines; they have the force of law. We also refer to good laboratory practice as GLP. GLP is part of the quality assurance that ensures that organizations consistently produce and control goods to a high quality standard. Good laboratory practice is not only concerned with production, but also quality control.What are the principles of Good Laboratory Practice (GLP)?
“The principles of Good Laboratory Practice (GLP) promote the quality and validity of data generated in the testing of chemicals and prevent fraudulent practices.” Non-clinical good laboratory practice also refers to experimental research. The term refers to a quality system of management controls for laboratories where research is taking place.What is the history of Good Laboratory Practice?
In 1972, New Zealand was the first country to introduce good laboratory practice. The United States subsequently followed in 1978 after the Industrial BioTest Laboratories (IBT Labs) scandal. IBT Labs had been engaging in extensive scientific misconduct, including fraud. IBT Labs’ President and several top executives were indicted.What is the laboratory medicine Best Practices Initiative?
The Centers for Disease Control and Prevention’s (CDC) Division of Laboratory Systems (DLS) has sponsored the Laboratory Medicine Best Practices (LMBP) Initiative to address the need for a systematic, multidisciplinary, comprehensive, and transparent approach to identifying, evaluating, and recommending best practices for the field.