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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
Productivity and Economic Advantages of Coupling Single-Pass Tangential Flow Filtration to Multi-Column Chromatography for Continuous Processing
Mark Schofield, Ph.D., Karl Rogler, Xhorxhi Gjoka, Engin Ayturk, Ph.D., and René Gantier, Ph.D.
Cleanability and Re-Usability of Cadence™ Inline Diafiltration Modules
Navigating Technology Transfer
Enabling Total Biopharma Solutions
Pall Life Sciences
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FDA approves subcutaneous SKYRIZI induction regimen for Crohn’s disease
Ris-Rez cuts progression risk by 67% in Phase III relapsed osteosarcoma trial
Sofe-M combination shows 79% response rate in platinum-sensitive ovarian cancer
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Upcoming Webinars
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Mixed mode Chromatography in Purifying biologics – Overview
Presented by Vivek Halan, Senior Scientific manager at Zumutor Biologics Pvt Ltd
15th November 2018
Establishing Early Development Strategies For Therapeutics Proteins
Presented by Sorina Morar-Mitrica, Principal Fellow Sr Drug Product Lead Early Phase Biologics at Novartis and Bernardo Cordovez, PhD, Chief Science Officer & Founder, Halo Labs
21st October 2020
Mapping Future Technology Needs For Real Time Release Testing
Presented by Dr Udayanath Aich, Associate Director at Bristol-Myers Squibb
09th August 2019
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Featured Video
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
Amsphere TM A3
From Compliance to Circularity: Three Ways Pharma Manufacturers Can Rethink Resource Management
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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