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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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JSR Life Sciences
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Choice of Upstream Bioreactor Technologies for Industrial Scale Viral Manufacturing (White Paper USD3244)
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Overcoming Obstacles in AAV Viral Vector Manufacturing
Enabling Total Biopharma Solutions
Pall Life Sciences
Benefits of Mixed-Mode Cation Exchange Chromatography: CMM HyperCel™ Sorbent Used for Monoclonal Antibody and Other Recombinant Protein Purification
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Novartis’s Cosentyx® receives positive CHMP opinion for treating polymyalgia rheumatica
FDA approves Kerendia for chronic kidney disease linked to type 1 diabetes
Robigo raises Series A led by Leaps by Bayer to advance engineered crop protection biologicals
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Upcoming Webinars
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Designing production facilities of the future
Presented by Geoffrey Hodge, Chief Technical Officer at Unum Therapeutics and Gary M. Pigeau, Ph.D., Director - Centre for Advanced Therapeutic Cell Technologies at GE Healthcare
30th July 2019
Using In-Vitro Dissolution to Support Post Approval Changes Global Regulatory Expectations
Presented by Xin Bu, Principal Scientist at Bristol-Myers Squibb
05th February 2019
Operational Excellence in Process Development in Drug Substance Production
Presented by Ken Green, Ph.D, Head of Manufacturing, Science and Technology at Samsung Biologics, Klaus Mauch, CEO at Insilico Biotechnology AG
11th February 2021
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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
Amsphere TM A3
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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