Practical Monte Carlo Simulation in GMP Manufacturing and Control
Quantitative Tools for Understanding Variability, Uncertainty, and Risk in Pharmaceutical Production and Testing
Taylor & Francis Ltd
ISBN 978-1-041-36256-2
Standardpreis
Bibliografische Daten
Buch. Hardcover
2027
In englischer Sprache
Umfang: 280 S.
Format (B x L): 15.6 x 23.4 cm
Verlag: Taylor & Francis Ltd
ISBN: 978-1-041-36256-2
Produktbeschreibung
In pharmaceutical manufacturing, quality control, and quality assurance, critical GMP decisions are often made with incomplete data, variable processes, and uncertain measurements. Batch release, process validation, continued process verification, analytical data interpretation, sampling decisions, and stability assessment all require more than a deterministic "pass/fail" view. This book introduces Monte Carlo simulation as a practical framework for converting variability, uncertainty, and risk into quantitative, decision-relevant information.
Unlike general texts on simulation or pharmaceutical quality systems, this book focuses specifically on GMP manufacturing and control. It connects statistical modeling with real pharmaceutical problems, showing how stochastic simulation, bootstrap methods, uncertainty propagation, and predictive risk analysis can complement traditional QA/QC tools and support transparent, scientifically defensible decisions.
Key features include:
- Practical Monte Carlo case studies including assay, dissolution, process validation, CPV, stability, sampling plans, microbiological counts, capability, and measurement uncertainty
- Reproducible examples in R, requiring no proprietary statistical software
- Clear distinction between variability and uncertainty, with direct GMP interpretations
- Coverage of OOS probability, confidence intervals, non-normal data, overdispersion, bootstrap capability, empirical OC curves, expected loss, and predictive control
- Quantitative support for comparability assessments, manufacturing changes, and post-approval lifecycle decisions
- Alignment with modern risk-based thinking, including ICH Q9/Q10/Q11/Q14, FDA process validation, and USP <1210>/<1220>1220>1210>
Written for QA/QC professionals, manufacturing and process engineers, regulators, and statisticians in pharmaceutical and chemical-pharmaceutical environments, the book is a practical companion for moving from qualitative risk descriptions to quantitative, reproducible decision support. Its central message is simple: better GMP decisions can be made when uncertainty is explicitly modeled rather than ignored.
Autorinnen und Autoren
Produktsicherheit
Hersteller
Libri GmbH
Europaallee 1
36244 Bad Hersfeld, DE
gpsr@libri.de
BÜCHER VERSANDKOSTENFREI INNERHALB DEUTSCHLANDS
