良好实验室规范(GLP):分析化学家概述

IF 0.7 4区化学 Q4 CHEMISTRY, ANALYTICAL

Lc Gc North America Pub Date : 2023-10-01 DOI:10.56530/lcgc.na.un1878g5

Leon Doneski, David Roos, Michael Dong

引用次数: 1

摘要

良好实验室规范(GLP)是一项监管要求，旨在帮助确保药物开发过程中药理学和毒理学研究的质量、可靠性和完整性。本文概述了GLP法规和相关公共标准，重点介绍了与分析和生物分析化学家相关的实践。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Good Laboratory Practice (GLP): An Overview for the Analytical Chemist

Good Laboratory Practice (GLP) is a regulatory requirement to help ensure the quality, reliability, and integrity of pharmacological and toxicological studies during drug development. This article overviews GLP regulations and related public standards, focusing on practices relevant to analytical and bioanalytical chemists.

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来源期刊

Lc Gc North America 化学-分析化学

CiteScore

1.00

自引率

55.60%

发文量

审稿时长

2 months

期刊介绍： Founded in 1983, LCGC is the leading provider of digital and print content to the separation science market, enhancing the productivity, efficiency, and the overall value of separation techniques globally. Founded in 1983, LCGC is the leading provider of digital and print content to the separation science market, enhancing the productivity, efficiency, and the overall value of separation techniques globally. With our commitment to editorial excellence we have pioneered innovation across a broad portfolio of digital and print platforms.