Manufacturing of Quality Oral Drug Products: Processing and Safe Handling of Active Pharmaceutical Ingredients (API)

This book provides an understanding of what is required to engineer and  manufacture drug products. It bridges established concepts and provides  for a new outlook by concentrating and creating new linkages in the  implementation of manufacturing, quality assurance, and business  practices related to drug manufacturing and healthcare products.

This  book fills a gap by providing a connection between drug production and  regulated applications. It focuses on drug manufacturing, quality  techniques in oral solid dosage, and capsule filling including equipment  and critical systems, to control production and the finished products.  The book offers a correlation between design strategies and a  step-by-step process to ensure the reliability, safety, and efficacy of  healthcare products. Fundamentals of techniques, quality by design, risk  assessment, and management are covered along with a scientific method  approach to continuous improvement in the usage of computerized  manufacturing and dependence on information technology and control  operations through data and metrics.

Manufacturing and Quality  Assurance of Oral Pharmaceutical Products: Processing and Safe Handling  of Active Pharmaceutical Ingredients (API) is of interest to  professionals and engineers in the fields of manufacturing engineering,  quality assurance, reliability, business management, process, and  continuous improvement, life cycle management, healthcare products  manufacturing, pharmaceutical processing, and computerized  manufacturing.