Pharmaceutical Quality by Design
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Pharmaceutical Quality by Design: From Formulation Development to Process Optimization
Quality by Design (QbD) represents a systematic, science-driven approach to pharmaceutical development, emphasizing product understanding, risk assessment, and process optimization to support consistent quality.
This book presents a practical academic introduction to Pharmaceutical Quality by Design, connecting fundamental principles with key concepts in formulation development, critical quality attributes, critical process parameters, risk management, Design of Experiments (DoE), and process control. It explores how a structured, knowledge-based approach can strengthen pharmaceutical development and support informed decision-making throughout the product lifecycle.
Designed for pharmacy students, postgraduate scholars, researchers, academicians, and pharmaceutical professionals, this book aims to make essential QbD concepts accessible and relevant to contemporary pharmaceutical sciences. It provides a foundation for understanding the relationship between formulation variables, manufacturing processes, product performance, and quality requirements.
Whether you are building your academic knowledge or exploring modern pharmaceutical development strategies, this book offers a valuable starting point for understanding the principles and practical significance of Quality by Design.