正态分布属性使用公差区间设定产品规格的统计考虑。

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Chang Chen, Yi Tsong, Xutong Zhao, Meiyu Shen
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引用次数: 0

摘要

通常,假设质量数据是正态分布的,产品质量规范和控制图极限被确定为正负3个样本标准差的平均值。这些极限对应于以平均值为中心的区间,约占人口的97.3%。这一区间的估计值称为β含量容忍区间。建议采用双单侧β含量耐受区间法确定药品质量标准。对于给定的置信水平1-α和覆盖率百分比p,当样本量较小时,β含量公差区间不精确。为了推导出精确的β含量耐受区间,Faulkenberry和Daly提出了一个确定样本量的“优度”标准。为了避免在p较大时高估β含量的容忍区间,我们建议将精度要求定义为容忍区间覆盖1+p2以上的概率限制在预先指定的显著性水平α'上。质量规范研究通常没有计划适当的样本量。为了获得精确的β含量耐受区间,满足“优度”标准的适当覆盖率p和最小样本量也用预先指定的显著性水平α'确定。通过这种方法,可以适当地设置产品规格,同时避免过度规定质量限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Statistical considerations for using tolerance interval to set product specification for normally distributed attribute.

Conventionally, the product quality specification and control chart limits are determined as the mean plus and minus 3 sample standard deviations with the assumption that the quality data is normally distributed. These limits correspond to an interval centered at the mean, covering approximately 97.3% of the population. The estimate of such an interval is called the β-content tolerance interval. It has been proposed to use a two one-sided β-content tolerance interval approach for determining drug product quality specifications. For a given confidence level, 1-α, and a coverage percentage p, the β-content tolerance interval is not precise when the sample size is small. For the derivation of a precise β-content tolerance interval, Faulkenberry and Daly proposed a "goodness" criterion for sample size determination. In order to avoid overestimating the β-content tolerance interval when p is large, we propose to define the precision requirement as the probability of the tolerance interval covering more than 1+p2 is restricted to a pre-specified significance level α'. Quality specification studies are often not planned with proper sample sizes. To obtain precise β-content tolerance intervals for quality specification studies, the proper coverage p satisfying the "goodness" criterion and the minimum sample sizes were also determined with the pre-specified significance level α'. With this approach, one may properly set the product specificationwhile avoiding over-specifying the quality limits.

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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
期刊介绍: The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers: Drug, device, and biological research and development; Drug screening and drug design; Assessment of pharmacological activity; Pharmaceutical formulation and scale-up; Preclinical safety assessment; Bioavailability, bioequivalence, and pharmacokinetics; Phase, I, II, and III clinical development including complex innovative designs; Premarket approval assessment of clinical safety; Postmarketing surveillance; Big data and artificial intelligence and applications.
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