MANUFACTURING OF QUALITY ORAL DRUG PRODUCTS PROCESSING AND SAFE HANDLING OF ACTIVE PHARMACEUTICAL INGREDIENTS (HB 2022) Paperback

This book offers an understanding of the engineering and manufacturing processes required for drug products. It connects established concepts with new perspectives by focusing on creating links between manufacturing, quality assurance, and business practices in drug production and healthcare product development. By addressing a gap in the literature, it bridges the gap between drug manufacturing and regulatory applications. The book delves into oral solid dosage production, capsule filling, and the equipment and systems necessary to control production and ensure quality in finished products. It highlights the relationship between design strategies and step-by-step processes to ensure the safety, reliability, and efficacy of healthcare products. The text covers key techniques, quality by design principles, risk management, and continuous improvement strategies using computerized manufacturing, information technology, and data-driven control operations. "Manufacturing and Quality Assurance of Oral Pharmaceutical Products" is ideal for professionals and engineers in manufacturing engineering, quality assurance, process improvement, pharmaceutical processing, and healthcare product manufacturing.