Biopharmaceutical Processing, Development, Design, and Implementation of Manufacturing Processes

Biopharmaceutical Processing: Development, Design, and Implementation of Manufacturing Processes covers bioprocessing from cell line development to bulk drug substances. The methods and strategies described are essential learning for every scientist, engineer or manager in the biopharmaceutical and vaccines industry.

The integrity of the bioprocess ultimately determines the quality of the product in the biotherapeutics arena, and this book covers every stage including all technologies related to downstream purification and upstream processing fields. Economic considerations are included throughout, with recommendations for lowering costs and improving efficiencies. Designed for quick reference and easy accessibility of facts, calculations and guidelines, this book is an essential tool for industrial scientists and managers in the biopharmaceutical industry.

Key Features

• Offers a comprehensive, go-to reference for daily work decisions
• Covers both upstream and downstream processes
• Includes case studies that emphasize financial outcomes
• Presents summaries, decision grids, graphs and overviews for quick reference

Readership

Chemical/biochemical/bioprocess engineers, process chemists, analytical chemists, molecular biologists, microbiologists, biochemists/ biotechnologists, virologists, graduate-level students in these disciplines

Table of Contents

1. Overview of Biotherapeutics and Vaccine Industry
2. Industrial Process Design Concepts
3. Single-Use Concepts in Manufacturing
4. Equipment and Automation
5. Facility Design
6. Process Development Routines
7. Production Sources and their Selection
8. Upstream Processing
9. Downstream Processing 1: Recovery Process
10. Downstream Processing 2: Purification Process
11. Downstream Related Methods
12. Analytics
13. Regulatory Aspects
14. Manufacturing Operations
15. Economics