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Presents and discusses the vital precepts underlying the efficient, effective, and cost-effective development of pharmaceutical drug products. It focuses on the adoption of systematic quality principles of pharmaceutical development, which is imperative in achieving continuous improvement in end-product quality and also leads to reducing cost, time, and effort, while meeting regulatory requirements. Key features: Reviews a vast collection of literature on applicability of systematic product development tools Discusses various dosage forms where challenges are very high Provides regulatory guidance related to specific dosage form development Covers the major types of drug products, including enteral, parenteral, and other (including transdermal, inhalation, etc.)