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Application of Quality Risk Management to Process Validation
Robert Dream, Managing Director, HDR Company LLC
A Holistic Phase Appropriate Strategy for HCP-Limits and HCP Characterization
Dr. Markus Haindl, Global Head Gene Therapy Technical Research & Development, Roche Di...
Strategies for Extractable and Leachable Risk Assessment of Polymeric Single Use Systems U...
Ping Wang, Director, Johnson & Johnson
Use of Non-Contact Raman Spectroscopy to Derive Reaction Kinetics
Richard Hart, Senior Director – Head of Automation and Data Science (Previously Asso...
Amsphere A3
JSR Life Sciences
Featured Articles
Endotoxin Control Strategies for Parenteral Drug Product Manufacturing
Robert Simler Associate Director, Engineering and Technology Biogen, Cambridge, MA, USA
Expanding Adoption of Single-Use Systems Drives Need for Wider Range of Sterile Connector Technologies
James Barry, Director of Marketing, Americas, Pall Biotech
Coupling single-pass TFF before loading onto a chromatography sorbent
Cleanability and Re-Usability of Cadence™ Inline Diafiltration Modules
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FDA approves Kerendia for chronic kidney disease linked to type 1 diabetes
Körber certifies ZETA’s INOSIM Foresight for PAS X MES data integration
Novo Nordisk and Anthropic to team up on accelerating drug discovery through Claude
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Upcoming Webinars
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Current Progress in Approaches for The Safety Assessment of Extractables and Leachables
Presented by Kim Li, PhD, DABT, MPH, Amgen Inc. and Erica J. Tullo, Technology Manager, E&L - Analytical Labs, West Pharmaceutical Services
06th April 2018
Using In-Vitro Dissolution to Support Post Approval Changes Global Regulatory Expectations
Presented by Xin Bu, Principal Scientist at Bristol-Myers Squibb
05th February 2019
Accelerating the development of regenerative therapies: Large scale expansion of human mesenchymal stem cells
Presented by Jon Rowley, Ph.D. & Mark Szczypka, Ph.D.
28th March 2017
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Featured Video
At Pall we help you select the process model that’s perfect for you. Ensuring it’s adapted to meet your precise needs and assembled flawlessly, ready for the future, from day one.
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Technical Papers
From Compliance to Circularity: Three Ways Pharma Manufacturers Can Rethink Resource Management
Column Packing Protocol for Amsphere A3
Push-Button Simplicity: Automatic Fermentation with the BioFlo® 120 Auto Culture Mode
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Featured Products
Decrease Cleaning Validation Time and Resources
AdvantaPure
Amsphere™ A3 Protein A Resin – JSR Life Sciences
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