Skip to content
Scan a barcode
Scan
Paperback Practical Monte Carlo Simulation in GMP Manufacturing and Control: Quantitative Tools for Understanding Variability, Uncertainty, and Risk in Pharmace Book

ISBN: 1041362609

ISBN13: 9781041362609

Practical Monte Carlo Simulation in GMP Manufacturing and Control: Quantitative Tools for Understanding Variability, Uncertainty, and Risk in Pharmace

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 /

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.

Recommended

Format: Paperback

$80.99
Releases 12/28/2026

Customer Reviews

0 rating
Copyright © 2026 Thriftbooks.com Terms of Use | Privacy Policy | Do Not Sell/Share My Personal Information | Cookie Policy | Cookie Preferences | Accessibility Statement
ThriftBooks ® and the ThriftBooks ® logo are registered trademarks of Thrift Books Global, LLC
GoDaddy Verified and Secured