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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...
Amsphere A3
JSR Life Sciences
Featured Articles
Characterization and Engineering Performance of the Allegro™ STR 500 Single-Use Stirred Tank Bioreactor
Best Practices For Successful Filter Integrity Testing Using Water Intrusion Test (WIT) Method
Monica Cardona and Ian Johnson Pall Life Sciences
Single-Use-Systems: Leachable Study Design for Single-Use Components
Kathryn McGohan,Scientist, Global Manufacturing Sciences & Technology organization at Bristol-Myers Squibb
Cleanability and Re-Usability of Cadence™ Inline Diafiltration Modules
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FDA grants Priority Review to uniQure’s Huntington’s disease gene therapy
Roche launches VENTANA BAP1 test to support mesothelioma diagnosis
Shockwave Javelin IVL catheter shows positive results in pivotal FORWARD CAD study
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Upcoming Webinars
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Pharmaceutical Forensics for Safe Manufacturing and Supply
Presented by Ravi Kalyanaraman, Director at Bristol-Myers Squibb and Jeremy Peters, Scientist at Bristol-Myers Squibb and Dr. Robert Heintz, Senior Applications Specialist at Thermo Fisher Scientific
14th June 2019
Considerations on Impact of Raw Material Variability in Gene Therapy Manufacturing: Applying Lessons Learned From Biologics Manufacturing
Presented by Presented by Aaron Mack, Engineer at Biogen and and Greg Stromberg Interim Leader of Global Manufacturing Material Sciences at Biogen,, Dr Lisa Dixon, Acting National Director, Animal Product Import and Export at US DA
22nd October 2020
Lessons Learned and Benefits Gained from the Global Implementation of an Automated Endotoxin Testing Solution
Presented by Dennis Wong, Global QC Technical Lead, Global Quality Control, Operations, AstraZeneca Liverpool UK
09th March 2023
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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
Column Packing Protocol for Amsphere A3
Caustic Stability of Amsphere A3 : Cycling Study with 0.5 M NaOH
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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Amsphere™ A3 Protein A Resin – JSR Life Sciences
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