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- W3005528908 abstract "In 1972, there were some cases of poor laboratory practice in the United States. Therefore, the FDA decided to do some in-depth researches of 40 toxicology laboratories and increase the number of laws for chemical and pharmaceutical products [1]. They discovered a lot of fraudulent activities and poor laboratory practices such as uncalibrated equipment, wrong measurements, inaccurate data, and inadequate test systems. Accordingly, by setting GLP guidelines, final data can demonstrate a true reflection of results gained during the study [2]. One of the important goals of GLP is promoting safety, quality, consistency, and reliability of products, data, and services in the process of laboratory testing, to improve human health and environmental risk management. Moreover, it is important to know how scientists use quality setting to improve biological products and data. Finally, research authorities should prove that there are no changes in the quality of data [1, 3]." @default.
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- W3005528908 date "2020-01-01" @default.
- W3005528908 modified "2023-10-18" @default.
- W3005528908 title "Principles of Good Laboratory Practice (GLP)" @default.
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- W3005528908 doi "https://doi.org/10.1007/978-3-030-35626-2_3" @default.
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