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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

Camzyos shows sustained benefit through 56 weeks in paediatric obstructive HCM

Livdelzi improves ALP normalisation rates in Phase III PBC study

Regeneron CIDEBsiRNA delivers up to 80% liver fat reduction in early MASLD study

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Upcoming Webinars

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Past Webinars

In Depth Characterization with Mass Spectrometry and Orthogonal Methods of Conformers in a Trispecific HIV Antibody

Presented by Bruno Genet, Lab head Structural Analysis MS at Sanofi
18th November 2020

Implementation Strategies and Challenges for Single-Use Technologies at Commercial Scale

Presented by Adam Goldstein, Roche/Genentech and Jacob McNeil, Thermo Fisher Scientific
17th May 2018

FDA Perspective on Aseptic Process Simulation for Cell Therapy Product Manufacturing

Presented by Lily Koo, Consumer Safety Officer at Food and Drug Administration and Keen Chung, Principal Scientist (Upstream Process) at Pall Biotech, Analytics Lead
16th October 2019

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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

Amsphere TM A3

Amsphere A3 – protein A resin: an optimized media to minimize the impact of elution buffer selection

Caustic Stability of Amsphere A3 : Cycling Study with 0.5 M NaOH

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