ABSTRACT

Continuous manufacturing of pharmaceuticals, including aspects of modern process development is highlighted in this book with both the ‘why’ and the ‘how’, emphasizing process modeling and process analytical technologies. Presenting specific case studies and drawing upon extensive experience from industry and academic opinion leaders, this book focuses on the practical aspects of continuous manufacturing. It gives the readers the strategic perspective and technical depth needed to adopt and implement these technologies, where appropriate, in order to gain the competitive edge in speed, agility, and reliability.

Features:

  • Discusses scientific solutions and process analytical technology to enable continuous manufacturing in the development of new drugs
  • Includes short stories about how some companies have adopted CM and what their drivers were and what benefits were realized
  • Addresses economic and practical considerations, unlike many other technical books
  • Emphasizes the practical aspects to give the reader the strategic imperative and technological depth to adopt and implement these technologies
  • Highlights the "why" and the "how", focusing on the need analysis and process modeling and process analytical technologies

part I|270 pages

Design and Control

chapter 1|83 pages

A Survey of Continuous API Syntheses

Insights at the Interface of Chemistry and Chemical Engineering

part II|37 pages

Design and Control

chapter 8|12 pages

Continuous Manufacturing of Biologics Drug Products

Challenges of Implementing Innovation in cGMP

chapter 9|23 pages

Modernizing Manufacturing of Parenteral Products

From Batch to Continuous Lyophilization

part IV|103 pages

Modeling, Design Space, and Future Outlook

chapter 13|15 pages

End-to-End Design Space for Continuous Manufacturing of Pharmaceuticals

Understanding Interactions Across Integrated Continuous Operations