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

This book provides an understanding of drug engineering and manufacturing, bridging established concepts and creating new linkages in implementation. It focuses on oral solid dosage, capsule filling, and quality assurance, offering a step-by-step process to ensure reliability, safety, and efficacy. It is of interest to professionals and engineers in various fields.

Format: Hardback
Length: 188 pages
Publication date: 27 June 2022
Publisher: Taylor & Francis Ltd

This comprehensive book provides a thorough understanding of the essential elements required for engineering and manufacturing drug products. By seamlessly bridging established concepts and forging new connections in the implementation of manufacturing, quality assurance, and business practices related to drug manufacturing and healthcare products, it offers a fresh perspective.

The book fills a crucial gap by establishing a connection between drug production and regulated applications. It delves into drug manufacturing, quality techniques in oral solid dosage, and capsule filling, including equipment and critical systems, to control production and ensure the quality of the finished products. Moreover, the book offers a valuable correlation between design strategies and a step-by-step process to guarantee 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 utilization of computerized manufacturing and reliance 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 immense interest to professionals and engineers working 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.

This comprehensive book offers a thorough exploration of the indispensable components necessary for engineering and manufacturing drug products. By seamlessly bridging established concepts and forging new connections in the implementation of manufacturing, quality assurance, and business practices related to drug manufacturing and healthcare products, it presents a fresh perspective.

The book fills a crucial gap by establishing a connection between drug production and regulated applications. It delves into drug manufacturing, quality techniques in oral solid dosage, and capsule filling, including equipment and critical systems, to control production and ensure the quality of the finished products. Moreover, the book offers a valuable correlation between design strategies and a step-by-step process to guarantee 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 utilization of computerized manufacturing and reliance 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 immense interest to professionals and engineers working 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.

Dimension: 234 x 156 (mm)
ISBN-13: 9781032124735