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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

Ris-Rez cuts progression risk by 67% in Phase III relapsed osteosarcoma trial


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


Mo-Rez shows 62% response rate in platinum-resistant ovarian cancer


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Upcoming Webinars

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Past Webinars

Qualification of Raw Materials and Cell Substrates for Biomanufacturing

Presented by Maura C. Kibbey, Ph.D., Director, Science & Standards, Global Biologics, U.S. Pharmacopeia and Martin Wisher, PhD, Global Head of Regulatory Affairs at Merck
16th January 2020


Raman spectroscopy measurements during Bioprocessing

Presented by Nobel Vale, Research Scientist II, Bristol-Myers Squibb and Justin Moretto, Bioprocessing Consultant, Kaiser Optical Systems, Inc.
11th July 2018


Challenges and Successes in Externalization of the ADC Supply Chain

Presented by Firelli Alonso, Ph.D., Pfizer
14th February 2017


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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

Rationale Design of Valves for Flexible Processing


Column Packing Protocol for Amsphere A3


Strategy Emerging Markets for Risk Mitigation


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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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