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GLP: Good Laboratory Practice

Abstract
Standards for laboratory investigations; GLP principles are defined by the EC (I) as: “principles of good laboratory practice, that are consistent with the OECD principles of good laboratory practice as adopted in article 1 of directive 87/18/EEC”.


GLP: Good Laboratory Practice
Isin Akyar
Acibadem University Faculty of Medicine Department of Medical Microbiology
Turkey
1. Introduction
In the early 70’s FDA (United States Food and Drug administration) have realized cases of
poor laboratory practice throughout the United States. FDA decided to check over 40
toxicology labs in-depth. They revealed lot dishonest activities and a lot of poor lab
practices. Examples of some of these poor lab practices found were equipment not been
calibrated to standard form, therefore giving wrong measurements, incorrect or inaccurate
accounts of the actual lab study and incompetent test systems. Although the term “good
laboratory practice” might have been used informal already for some time in many
laboratories around the world GLP originated in the United States and it had a powerfull
effect world wide.



https://www.researchgate.net/publication/221919330_GLP_Good_Laboratory_Practice

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