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评估国际协调会议(ICH)有效期估算指南的性能。

Evaluating the performance of the ICH guidelines for shelf life estimation.

作者信息

Quinlan Michelle, Stroup Walter, Schwenke James, Christopher David

机构信息

Novartis Oncology, Florham Park, NJ 07932, USA.

出版信息

J Biopharm Stat. 2013;23(4):881-96. doi: 10.1080/10543406.2013.789889.

Abstract

The goal of shelf life estimation is to determine the storage time during which the entire product meets specification with acceptably high probability. The estimated shelf life should be "applicable to all future batches" (ICH Q1E, International Conference on Harmonization, 2003b). There is compelling evidence of issues with the International Conference on Harmonization (ICH) guidelines for shelf life estimation. Issues include fixed batch effects, poolability tests, and confidence intervals for the mean. Two conclusions from evaluating the ICH procedure are that batch effects should be random and that focus should be on a quantile. A procedure is needed that combines random batches with the ICH objective of estimating the minimum batch shelf life.

摘要

保质期估计的目标是确定在整个产品以可接受的高概率符合规格的储存时间。估计的保质期应“适用于所有未来批次”(国际协调会议(ICH)Q1E,2003b)。有令人信服的证据表明国际协调会议(ICH)的保质期估计指南存在问题。这些问题包括固定批次效应、合并性测试以及均值的置信区间。评估ICH程序得出的两个结论是批次效应应该是随机的,并且重点应该放在分位数上。需要一种将随机批次与估计最小批次保质期的ICH目标相结合的程序。

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