{"title":"Statistical considerations for using tolerance interval to set product specification for normally distributed attribute.","authors":"Chang Chen, Yi Tsong, Xutong Zhao, Meiyu Shen","doi":"10.1080/10543406.2025.2473612","DOIUrl":null,"url":null,"abstract":"<p><p>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 <math><mi>β</mi></math>-content tolerance interval. It has been proposed to use a two one-sided <math><mi>β</mi></math>-content tolerance interval approach for determining drug product quality specifications. For a given confidence level, <math><mn>1</mn><mo>-</mo><mi>α</mi><mo>,</mo></math> and a coverage percentage <i>p</i>, the <math><mi>β</mi></math>-content tolerance interval is not precise when the sample size is small. For the derivation of a precise <math><mi>β</mi></math>-content tolerance interval, Faulkenberry and Daly proposed a \"goodness\" criterion for sample size determination. In order to avoid overestimating the <math><mi>β</mi></math>-content tolerance interval when <i>p</i> is large, we propose to define the precision requirement as the probability of the tolerance interval covering more than <math><mrow><mfrac><mrow><mfenced><mrow><mn>1</mn><mo>+</mo><mi>p</mi></mrow></mfenced></mrow><mn>2</mn></mfrac></mrow></math> is restricted to a pre-specified significance level <math><msup><mi>α</mi><mo>'</mo></msup></math>. Quality specification studies are often not planned with proper sample sizes. To obtain precise <math><mi>β</mi></math>-content tolerance intervals for quality specification studies, the proper coverage <i>p</i> satisfying the \"goodness\" criterion and the minimum sample sizes were also determined with the pre-specified significance level <math><msup><mi>α</mi><mo>'</mo></msup></math>. With this approach, one may properly set the product specificationwhile avoiding over-specifying the quality limits.</p>","PeriodicalId":54870,"journal":{"name":"Journal of Biopharmaceutical Statistics","volume":" ","pages":"1-6"},"PeriodicalIF":1.2000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biopharmaceutical Statistics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10543406.2025.2473612","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
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 -content tolerance interval. It has been proposed to use a two one-sided -content tolerance interval approach for determining drug product quality specifications. For a given confidence level, and a coverage percentage p, the -content tolerance interval is not precise when the sample size is small. For the derivation of a precise -content tolerance interval, Faulkenberry and Daly proposed a "goodness" criterion for sample size determination. In order to avoid overestimating the -content tolerance interval when p is large, we propose to define the precision requirement as the probability of the tolerance interval covering more than is restricted to a pre-specified significance level . Quality specification studies are often not planned with proper sample sizes. To obtain precise -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 . With this approach, one may properly set the product specificationwhile avoiding over-specifying the quality limits.
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.