Current Issue
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
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.
Coupling single-pass TFF before loading onto a chromatography sorbent
Bringing the Freezing of Biopharmaceuticals in From the Cold
Volume Reduction and Process Optimization with Cadence Inline Concentrator
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TAK-881 matches HYQVIA exposure while reducing infusion volume in Phase II/III PID study
Roche highlights divarasib, giredestrant and Tam-Peli data ahead of ESMO 2026
ENTYVIO treat-to-target strategy reduces ulcerative colitis complication risk in Phase IV VERDICT trial
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Upcoming Webinars
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Pharmaceutical Hot Melt Extrusion A Cost Effective Method to Increase Solubility
Presented by Dennis Douroumis, Professor in Pharmaceutical Technology and Process Engineering at University of Greenwich and Dr.-Ing Margarethe Richter, Pharma Application Specialist at Thermo Fisher Scientific
07th May 2019
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
New Tools to Assess the Risk of Microbial Impurities in the Pharmaceutical Manufacturing Process
Presented by Dr Friedrich von Wintzingerode, Senior Manager, Global Analytical Science & Technology (gASAT) Microbiology, Global QC bei Roche and Mathilde Arnault, Research Scientist, BioMonitoring R&D, Merck KGaA, Darmstadt, Germany
09th April 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
Push-Button Simplicity: Automatic Fermentation with the BioFlo® 120 Auto Culture Mode
From Compliance to Circularity: Three Ways Pharma Manufacturers Can Rethink Resource Management
Rationale Design of Valves for Flexible Processing
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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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