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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
Choice of Upstream Bioreactor Technologies for Industrial Scale Viral Manufacturing (White Paper USD3244)
Pall Corporation
Coupling single-pass TFF before loading onto a chromatography sorbent
Process Analytical Technology For Upstream Bioprocessing
Erica Fratz-Berilla and Cyrus Agarabi, FDA CDER
Benefits of Mixed-Mode Cation Exchange Chromatography: CMM HyperCel™ Sorbent Used for Monoclonal Antibody and Other Recombinant Protein Purification
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FDA grants Priority Review to uniQure’s Huntington’s disease gene therapy
FDA approves Abbott’s Amplatzer Paraclose device for heart valve leaks
Roche launches VENTANA BAP1 test to support mesothelioma diagnosis
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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
Designer Sterile Filtration in Aseptic Processing Using Single Use Technology
Presented by Alan Kelly, Project Engineer at Sanofi and Terri Love, Senior BioManufacturing at Merck
10th November 2020
Real Time Monitoring of Bioprocess and Beyond – A Process Analytical Perspective
Presented by Dhanuka Wasalathanthri, Senior Scientist at Bristol Myers Squibb and Julia Ding, Head, Global Process Analytical Development at Bristol Myers Squibb and Eric Carlson, Ph.D., President & CEO, Protein Metrics Inc.
16th November 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
From Compliance to Circularity: Three Ways Pharma Manufacturers Can Rethink Resource Management
Best Practices for Achieving Virus Safety
Lifetime study for JSR Amsphere A3 – protein A resin
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Decrease Cleaning Validation Time and Resources
AdvantaPure
Amsphere™ A3 Protein A Resin – JSR Life Sciences
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