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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...
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Featured Articles
Bringing the Freezing of Biopharmaceuticals in From the Cold
Best Practices For Successful Filter Integrity Testing Using Water Intrusion Test (WIT) Method
Monica Cardona and Ian Johnson Pall Life Sciences
Enabling Total Biopharma Solutions
Pall Life Sciences
Navigating Technology Transfer
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Teva discontinues Phase II emrusolmin trial in multiple system atrophy after futility analysis
Intranasal foralumab reduces microglial activation in Phase IIa progressive MS trial
Impella registry analyses report lower mortality than CHIP-BCIS3 in high-risk PCI
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Upcoming Webinars
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Meaningful Metrics For The Microbiology Laboratory
Presented by Karen McCullough, Principal Consultant at MMI Associates
29th October 2014
Affinity Chromatography for Vaccines Purification
Presented by Mikkel Nissum, Vaccine R&D Quality Site Lead at GSK Vaccines
12th May 2020
End User Perspective on Setting in-Process Endotoxin Limits
Presented by Dr Friedrich von Wintzingerode, Roche/Genentech
15th May 2018
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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
Rationale Design of Valves for Flexible Processing
Push-Button Simplicity: Automatic Fermentation with the BioFlo® 120 Auto Culture Mode
Best Practices for Achieving Virus Safety
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Decrease Cleaning Validation Time and Resources
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Amsphere™ A3 Protein A Resin – JSR Life Sciences
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