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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



Headline News

Sofe-M combination shows 79% response rate in platinum-sensitive ovarian cancer


FDA expands TALZENNA plus XTANDI approval to earlier metastatic prostate cancer setting


JNJ-6143 shows 75% tumour response rate in Phase I advanced prostate cancer study


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Upcoming Webinars

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Past Webinars

Analytical Strategies for Comparability in Bioprocess Development

Presented by Dr Christine P. Chan, Ph.D., Sanofi. Followed by Joe Barco, Ph.D. Unchained Labs
28th March 2017


Meaningful Metrics For The Microbiology Laboratory

Presented by Karen McCullough, Principal Consultant at MMI Associates
29th October 2014


The Importance of Accurate Chemical Characterization of Medical Devices Extractables

Presented by Ron Brown, Toxicologist at Risk Science Consortium and Piet Christiaens, PhD, Scientific Director at Nelson Labs
16th November 2022


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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.

There’s no kit for the perfect biotech process. Until now.

 

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Technical Papers

Strategy Emerging Markets for Risk Mitigation


Column Packing Protocol for Amsphere A3


Best Practices for Achieving Virus Safety


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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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