Literature DB >> 19551518

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

Steven Novick1, David Christopher, Monisha Dey, Svetlana Lyapustina, Michael Golden, Stefan Leiner, Bruce Wyka, Hans-Joachim Delzeit, Chris Novak, Gregory Larner.   

Abstract

The FDA proposed a parametric tolerance interval (PTI) test at the October 2005 Advisory Committee meeting as a replacement of the attribute (counting) test for delivered dose uniformity (DDU), published in the 1998 draft guidance for metered dose inhalers (MDIs) and dry powder inhalers (DPIs) and the 2002 final guidance for inhalation sprays and intranasal products. This article (first in a series of three) focuses on the test named by the FDA "87.5% coverage." Unlike a typical two-sided PTI test, which controls the proportion of the DDU distribution within a target interval (coverage), this test is comprised of two one-sided tests (TOST) designed to control the maximum amount of DDU values in either tail of the distribution above and below the target interval. Through simulations, this article characterizes the properties and performance of the proposed PTI-TOST under different scenarios. The results show that coverages of 99% or greater are needed for a batch to have acceptance probability 98% or greater with the test named by the FDA "87.5% coverage" (95% confidence level), while batches with 87.5% coverage have less than 1% probability of being accepted. The results also illustrate that with this PTI-TOST, the coverage requirement for a given acceptance probability increases as the batch mean deviates from target. The accompanying articles study the effects of changing test parameters and the test robustness to deviations from normality.

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Year:  2009        PMID: 19551518      PMCID: PMC2802173          DOI: 10.1208/s12249-009-9270-x

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  4 in total

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

Authors:  W W Hauck; R Shaikh
Journal:  J Biopharm Stat       Date:  2001-11       Impact factor: 1.051

2.  Parametric two-stage sequential quality assurance test of dose content uniformity.

Authors:  Yi Tsong; Meiyu Shen
Journal:  J Biopharm Stat       Date:  2007       Impact factor: 1.051

3.  Parametric two-tier sequential quality assurance test of delivery dose uniformity of multiple-dose inhaler and dry powder inhaler drug products.

Authors:  Yi Tsong; Meiyu Shen; Richard T Lostritto; Guiragos K Poochikian
Journal:  J Biopharm Stat       Date:  2008       Impact factor: 1.051

4.  Comparison of criteria for content uniformity.

Authors:  B Flann
Journal:  J Pharm Sci       Date:  1974-02       Impact factor: 3.534

  4 in total
  2 in total

1.  Challenges and opportunities in implementing the FDA default parametric tolerance interval two one-sided test for delivered dose uniformity of orally inhaled products.

Authors:  Greg Larner; Andrew Cooper; Svetlana Lyapustina; Stefan Leiner; David Christopher; Helen Strickland; Michael Golden; Hans-Joachim Delzeit; Emil M Friedman
Journal:  AAPS PharmSciTech       Date:  2011-09-08       Impact factor: 3.246

2.  Tolerance interval testing for assessing accuracy and precision simultaneously.

Authors:  Chieh Chiang; Chin-Fu Hsiao
Journal:  PLoS One       Date:  2021-02-05       Impact factor: 3.240

  2 in total

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