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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
Scheduling and Optimization of Biomanufacturing Activities in Multi-product Facilities with Disposable Technologies
Gloria Gadea-Lopez, Ph.D. is Director of Production and Business Systems at the Shire Lexington, John Maguireis the Associate Director of Manufacturing Systems at Shire’s Lexington and Megan Rabideau is a Manufacturing Systems Engineer at Shire’s Lexington
Trends in Single-Use Mixing Technologies and Insight into Pall and Lonza Ibex® Solutions
Endotoxin Control Strategies for Parenteral Drug Product Manufacturing
Robert Simler Associate Director, Engineering and Technology Biogen, Cambridge, MA, USA
Enabling Total Biopharma Solutions
Pall Life Sciences
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Intranasal foralumab reduces microglial activation in Phase IIa progressive MS trial
Roche launches VENTANA BAP1 test to support mesothelioma diagnosis
FDA approves Abbott’s Amplatzer Paraclose device for heart valve leaks
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Upcoming Webinars
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Raw Material Lot Variability Challenges During Manufacturing of Biosimilars mab
Presented by Sekhar Reddy, DSP Lead for Biosimilars at Biocon MSAT
25th January 2019
Disposables – Suitability and Process Economy In Biopharmaceutical Manufacturing – A Reality Check
Presented by Joachim Walter
08th February 2018
Making Virus Inactivation a Reality for Continuous Upscaled Processes
Presented by Mark Schofield, Ph.D., Principal R&D Engineer, Pall Life Sciences - Westborough, MA, USA
30th November 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
From Compliance to Circularity: Three Ways Pharma Manufacturers Can Rethink Resource Management
Strategy Emerging Markets for Risk Mitigation
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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