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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
Navigating Technology Transfer
Trends in Single-Use Mixing Technologies and Insight into Pall and Lonza Ibex® Solutions
Continuous processing optimization with smarter tools
Barbara Paldus, Ph.D.
Vice President & General Manager Finesse, part of Thermo Fisher Scientific
Successful Wetting for Filter Integrity Testing in Volume-Restricted Systems
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Camzyos shows sustained benefit through 56 weeks in paediatric obstructive HCM
Zura Bio discontinues tibulizumab development in hidradenitis suppurativa after Phase II miss
Pasritamig combination delivers 73% PSA response rate in advanced prostate cancer Phase I study
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Upcoming Webinars
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Do Extractable Protocols Truly Help – An End User Perspective
Presented by Ekta Mahajan
05th February 2018
Creation of a real time process data framework with external manufacturer to enhance process performance, technology transfer success and drive cost savings
Presented by Olav Lyngberg, Advanced Analytics, Modeling & Process Analytical Technology Leader at The Janssen Pharmaceutical Companies of Johnson & Johnson
08th February 2023
Continuous Bioprocessing Solutions Webinar Series Part II
Presented by Moderator: Kevin Marino, Presenter: Jon Petrone
23rd May 2017
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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
Strategy Emerging Markets for Risk Mitigation
From Compliance to Circularity: Three Ways Pharma Manufacturers Can Rethink Resource Management
Push-Button Simplicity: Automatic Fermentation with the BioFlo® 120 Auto Culture Mode
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Decrease Cleaning Validation Time and Resources
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