The application of control charts in regulated bioanalysis for monitoring long-term reproducibility

Author:

Bruijnsvoort Michel van1,Meijer John1,den Beld Cas van1

Affiliation:

1. Astellas Pharma Europe B.V., Drug Development Research, Bioanalysis-Europe, Sylviusweg 62, 2333 BE Leiden, The Netherlands

Abstract

In regulated bioanalysis, the acceptance of results is batch-wise. When during clinical development derived pharmacokinetic or pharmacodynamic results from different studies will be combined or compared, it is recommendable to monitor the long-term reproducibility of bioanalytical assays. Long-term reproducibility can be evaluated by control charts generated from control samples included in each batch. We present a methodology for the implementation, construction and evaluation of control charts next to the regular batch acceptance of bioanalytical results. Decision rules can be set up for a statistical evaluation of the results. Violation of a decision rule may lead to a root-cause investigation and corrective actions to improve assay robustness. Three examples of control charts, for pharmacokinetic and pharmacodynamic analytes are presented.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

Reference36 articles.

1. Guideline on Bioanalytical Method Validation, European Medicines Agency (2012). www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2011/08/WC500109686.pdf.

2. Guidance for Industry – Bioanalytical Method Validation, U.S. Department of Health and Human Services, Food and Drug Administration Center for Drug Evaluation and Research (2001). www.fda.gov/downloads/Drugs/Guidance/ucm070107.pdf.

3. Fit-for-Purpose Method Development and Validation for Successful Biomarker Measurement

4. ICH M4E Guideline: Clinical Overview and Clinical Summary of Module 2 and Module 5: Clinical Study Reports (R1) [cited 2002 Sep 12]. www.ich.org/fileadmin/Public_Web_Site/ICH_Products/CTD/M4__R1__Efficacy/M4E__R1_.pdf.

5. Model-based Drug Development

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