Literature DB >> 12018783

Sample sizes for batch acceptance from single- and multistage designs using two-sided normal tolerance intervals with specified content.

W W Hauck1, R Shaikh.   

Abstract

One quality control test in the pharmaceutical industry is a test for uniformity of content of a batch prior to release of the batch to market. For batch acceptance by this or other quantitative tests of batch quality, one approach uses two-sided tolerance intervals of specified content. If the tolerance interval falls entirely within an acceptance interval, the batch is accepted. This has the form of a statistical hypothesis test. Once we recognize this approach as a statistical test, we can ask what sample size is required to be able to accept the batch with a desired power. The power for a single-stage design is a bivariate noncentral t probability and can be determined using previously published algorithms. Using standard methods for interim analyses, the approach is extended to multistage designs. Power and sample size for multistage designs are validated with simulations. We demonstrate it is possible to design one- and two-stage designs for batch acceptance with desired power and specified type I level.

Mesh:

Substances:

Year:  2001        PMID: 12018783

Source DB:  PubMed          Journal:  J Biopharm Stat        ISSN: 1054-3406            Impact factor:   1.051


  6 in total

Review 1.  Content uniformity and dose uniformity: current approaches, statistical analyses, and presentation of an alternative approach, with special reference to oral inhalation and nasal drug products.

Authors:  Roger L Williams; Wallace P Adams; Guirag Poochikian; Walter W Hauck
Journal:  Pharm Res       Date:  2002-04       Impact factor: 4.200

2.  Oral dosage form performance tests: new dissolution approaches.

Authors:  Walter W Hauck; Thomas Foster; Eric Sheinin; Todd Cecil; William Brown; Margareth Marques; Roger L Williams
Journal:  Pharm Res       Date:  2005-02       Impact factor: 4.200

3.  A total error approach for the validation of quantitative analytical methods.

Authors:  David Hoffman; Robert Kringle
Journal:  Pharm Res       Date:  2007-03-21       Impact factor: 4.200

4.  A two one-sided parametric tolerance interval test for control of delivered dose uniformity. Part 1--characterization of FDA proposed test.

Authors:  Steven Novick; David Christopher; Monisha Dey; Svetlana Lyapustina; Michael Golden; Stefan Leiner; Bruce Wyka; Hans-Joachim Delzeit; Chris Novak; Gregory Larner
Journal:  AAPS PharmSciTech       Date:  2009-06-24       Impact factor: 3.246

5.  Study of the applicabilty of content uniformity and dissolution variation test on ropinirole hydrochloride tablets.

Authors:  Edina Vranić; Alija Uzunović
Journal:  Bosn J Basic Med Sci       Date:  2008-05       Impact factor: 3.363

6.  Empirical study of employee loyalty and satisfaction in the mining industry using structural equation modeling.

Authors:  Shoukun Chen; Kaili Xu; Xiwen Yao
Journal:  Sci Rep       Date:  2022-01-21       Impact factor: 4.379

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.