Large-scale drug production requires an understanding of both formulation and manufacturing principles. This book introduces the basics of industrial pharmacy, covering unit operations, equipment handling, good manufacturing practices (GMP), and process validation. Topics such as tablet compression, granulation, coating, and packaging are explained with attention to quality assurance and regulatory standards. It also addresses scale-up issues and industrial problem-solving strategies. This resource supports students and professionals aiming to work in pharmaceutical production environments with a foundation in applied pharmaceutics.
Chesa Delgado is a pharmaceutical scientist with a primary focus on manufacturing processes, quality assurance, and regulatory compliance in drug production. With over a decade of experience in industrial settings, she has contributed to optimizing tablet compression, granulation methods, and stability testing. Her work frequently involves cross-functional collaboration between R&D and manufacturing units, aiming to ensure consistent product quality. Chesa is also known for her contributions to GMP training and production workflow optimization initiatives.