Continuous Manufacturing of Pharmaceuticals, Volume 65 in the Advances in Chemical Engineering series, explores the latest innovations in continuous manufacturing. This volume presents insightful chapters covering key topics such as the design of flow reactors for small molecule production, enabling technologies and equipment, continuous separations, and real-time monitoring using Quality-by-Design (QbD) and Process Analytical Technology (PAT). Additionally, it highlights the role of high-throughput experimentation, artificial intelligence integration, and regulatory considerations, offering a comprehensive outlook on the challenges and future perspectives of continuous pharmaceutical manufacturing.
Table of Contents
1. Introduction to Continuous Manufacturing of Pharmaceuticals2. Design of Flow Reactors and Applications in Small Molecules Production
3. Key Enabling Technologies and Equipment
4. Continuous Separations
5. Quality-by-Design (QbD), Process Analytical Technology (PAT), and Real-Time Monitoring
6. High-Throughput Experimentation and Integration with Artificial Intelligence
7. Regulatory Aspects of Continuous Manufacturing
8. Challenges and Future Perspectives
