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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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Headline News

FDA grants Priority Review to uniQure’s Huntington’s disease gene therapy


Impella registry analyses report lower mortality than CHIP-BCIS3 in high-risk PCI


FDA approves Abbott’s Amplatzer Paraclose device for heart valve leaks


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Past Webinars

Final Revised Version of BioPhorum Extractable Testing Recommendation Part 2

Presented by Sara Ullsten, R&D Section Manager, Cytiva and Haiyan Hong, R&D manager of Life Sciences at Saint-Gobain
11th June 2020


Advanced Raman Spectroscopy Beyond In-Process Glucose Control of Commercial Cell Culture Processes

Presented by Dan Hill, Manufacturing Scientist at Biogen and Maryann Cuellar, Life Science Product Manager at Kaiser Optical Systems, Inc.
03rd June 2020


Big Data Strategies for Cell Therapy Manufacturing

Presented by Scott R. Burger, MD, Principal, Advanced Cell & Gene Therapy, LLC And Heidi Hagen, Co-founder and Chief Strategy Officer for Vineti Inc
17th September 2019


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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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Amsphere TM A3


Best Practices for Achieving Virus Safety


Rationale Design of Valves for Flexible Processing


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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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