Opportunities and Future Growth of the CDMO Market
Process Related Impurities in Biologics – Best Practices, New Technologies, and Outsourcing
Multivariate Data Analysis in Biopharmaceutical Development
Cell Culture Media Designed for Intensified Perfusion Processes
Immediate, Flexible Capacity with Hydrated Buffers and Process Liquids
Immediate, Flexible Capacity with Hydrated Buffers and Process liquids
USP General Chapters and Reference Standards that Support the Development and Characterization of Biologics
Effective Technology Transfer Strategies for Biologic- Drug Development
Research Trends in Biopharma
Value of Standards for Biologics
The Changing Biopharma Regulatory Landscape
Effective Extractables and Leachables: Evaluation Programs for Single-Use Systems