Literature DB >> 14620848

Statistical tools for setting in-process acceptance criteria.

R J Seely1, L Munyakazi, J Haury.   

Abstract

Establishing meaningful and reasonable acceptance criteria for process validation or continual monitoring is crucial to approval and successful manufacturing. The limits should be based on statistical analysis of historical data when possible. The control limits of "mean +/- 3 standard deviations" is one industry standard. However, the limits may be artificially constraining if the standard deviation does not reflect the true variance of the process. Under-estimation of process variance is common with small data sets. This paper presents three methods for correcting underestimated variance, allowing the setting of acceptance criteria that are slightly larger than +/- 3 standard deviations. These limits are more meaningful in that they account for true process variability and will signal process deviations due only to a specific cause.

Mesh:

Year:  2003        PMID: 14620848

Source DB:  PubMed          Journal:  Dev Biol (Basel)        ISSN: 1424-6074


  3 in total

1.  Variation transmission model for setting acceptance criteria in a multi-staged pharmaceutical manufacturing process.

Authors:  Richard O Montes
Journal:  AAPS PharmSciTech       Date:  2011-12-23       Impact factor: 3.246

2.  Analytical similarity assessment of rituximab biosimilar CT-P10 to reference medicinal product.

Authors:  Kyoung Hoon Lee; Jihun Lee; Jin Soo Bae; Yeon Jung Kim; Hyun Ah Kang; Sung Hwan Kim; So Jung Lee; Ki Jung Lim; Jung Woo Lee; Soon Kwan Jung; Shin Jae Chang
Journal:  MAbs       Date:  2018-03-06       Impact factor: 5.857

3.  Specification-driven acceptance criteria for validation of biopharmaceutical processes.

Authors:  Lukas Marschall; Christopher Taylor; Thomas Zahel; Marco Kunzelmann; Alexander Wiedenmann; Beate Presser; Joey Studts; Christoph Herwig
Journal:  Front Bioeng Biotechnol       Date:  2022-09-23
  3 in total

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