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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
Novel Synthetic Adsorptive Depth Filter Media for CHO Harvest Clarification
John Amara, Ph.D. and Michael Dullen Merck, 80 Ashby Road, Bedford, MA, 01730, USA
Enabling Total Biopharma Solutions
Pall Life Sciences
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.
Trends in Single-Use Mixing Technologies and Insight into Pall and Lonza Ibex® Solutions
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FDA approves Abbott’s Amplatzer Paraclose device for heart valve leaks
Shockwave Javelin IVL catheter shows positive results in pivotal FORWARD CAD study
FDA places Bright Minds’ planned BMB-101 Phase II epilepsy study on partial clinical hold
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Upcoming Webinars
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Towards a lean Manufacturing: Implementing Single-Use Process Analytical Technologies (PAT) tools at the seed stage to simplify cell culture operations
Presented by Dr Jose R. Vallejos of Medimmune/AstraZeneca
24th May 2017
Just in Time Release of CAR T Cell Therapies During Covid-19
Presented by Irving Ford, Site QA Head multi-product CAR T facility at Bristol Myers Squibb and Lori Daane, Pharma Microbiology Scientific Director at bioMérieux
29th November 2021
Compression of film-coated pellets – key parameters for optimal tablet quality
Presented by Karl G. Wagner, Professor in Pharmaceutical Technology at the University of Bonn
04th March 2015
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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
Push-Button Simplicity: Automatic Fermentation with the BioFlo® 120 Auto Culture Mode
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Featured Products
Decrease Cleaning Validation Time and Resources
AdvantaPure
Amsphere™ A3 Protein A Resin – JSR Life Sciences
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