首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Harmonization of strategies for the validation of quantitative analytical procedures. A SFSTP proposal--part II.
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Harmonization of strategies for the validation of quantitative analytical procedures. A SFSTP proposal--part II.

机译:统一定量分析程序验证策略。 SFSTP提案-第二部分。

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As reported in a previous paper, the main objective of the new commission of the Societe Francaise des Sciences et Techniques Pharmaceutiques (SFSTP) was the harmonisation of approaches for the validation of quantitative analytical procedures. In a series of meetings, members of this Commission have first tried to review the objectives of analytical methods and the objectives of validation methods and to recommend the use of two-sided beta-expectation tolerance intervals for total error of validation samples (accuracy profile) in the acceptance/rejection of analytical method in validation phase. In the context of the harmonization, the other objectives were: (i) to propose a consensus on the norms usually recognized, while widely incorporating the ISO terminology; (ii) to recommend to validate the analytical procedure accordingly to the way it will be used in routine; (iii) to elaborate a rational, practical and statistically reliable strategy to assure the quality of the analytical results generated. This strategy has been formalised in a guide and the three latter objectives made by the Commission are summarised in the present paper which is the second part of summary report of the SFSTP commission. The SFSTP guide has been produced to help analysts to validate their analytical methods. It is the result of a consensus between professionals having expertise in analytical and/or statistical fields. The suggestions presented in this paper should therefore help the analyst to design and perform the minimum number validation experiments needed to obtain all the required information to establish and demonstrate the reliability of its analytical procedure.
机译:如前一篇论文中所述,法兴法国科学技术药学委员会(SFSTP)新委员会的主要目标是统一定量分析程序的验证方法。在一系列会议中,该委员会成员首先尝试审查分析方法的目的和验证方法的目的,并建议对验证样品的总误差(准确度分布图)使用双面β预期公差区间在验证阶段接受/拒绝分析方法。在统一的背景下,其他目标是:(i)在广泛采用ISO术语的同时,就通常公认的规范提出共识; (ii)建议按照常规使用的分析方法进行验证; (iii)制定合理,实用和统计可靠的策略,以确保产生的分析结果的质量。该战略已在指南中正式确定,委员会总结的后三个目标在本文件中得到了总结,这是SFSTP委员会摘要报告的第二部分。 SFSTP指南旨在帮助分析人员验证其分析方法。这是在分析和/或统计领域具有专业知识的专业人员之间达成共识的结果。因此,本文提出的建议应有助于分析人员设计和执行所需的最少数量的验证实验,以获取所有必需的信息,以建立并证明其分析程序的可靠性。

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