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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
Benefits of Mixed-Mode Cation Exchange Chromatography: CMM HyperCel™ Sorbent Used for Monoclonal Antibody and Other Recombinant Protein Purification
Choice of Upstream Bioreactor Technologies for Industrial Scale Viral Manufacturing (White Paper USD3244)
Pall Corporation
Endotoxin Control Strategies for Parenteral Drug Product Manufacturing
Robert Simler Associate Director, Engineering and Technology Biogen, Cambridge, MA, USA
Bringing the Freezing of Biopharmaceuticals in From the Cold
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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
Shockwave Javelin IVL catheter shows positive results in pivotal FORWARD CAD study
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Upcoming Webinars
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Mass Spectrometry – an Essential Tool for Characterization of Monoclonal Antibodies during Development
Presented by Dr Wei Xu & Dr Henry Shion
03rd February 2016
Analysing Complex Data in the Pharmaceutical Industry: The Case for Multivariate Analysis
Presented by Presented by Mike Tobyn, Research Fellow at Bristol-Myers Squibb
02nd May 2019
From Concept to Market – Unique Approaches in Biomanufacturing
Presented by Jincai Li, Vice President of WuXi Biologics and Kevin Mullen, Sr. Product Manager, Single-Use Systems at Thermo Fisher Scientific
11th September 2020
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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
Best Practices for Achieving Virus Safety
From Compliance to Circularity: Three Ways Pharma Manufacturers Can Rethink Resource Management
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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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