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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

Lilly and Hims & Hers expand access to Zepbound and Foundayo


Petosemtamab combination cuts risk of death by 50% in Phase III head and neck cancer trial


FDA grants Priority Review to uniQure’s Huntington’s disease gene therapy


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Past Webinars

Mechanistic Modelling in Early Stage Chromatography Process Development for Improving Process Efficiency and Productivity

Presented by Yuyi Shen, Associate Director, Process Development and Manufacturing at Bolt Therapeutics and Nick Whitelock, Business Development Manager at GoSilico GmbH
19th April 2021


End User Perspective on Setting in-Process Endotoxin Limits

Presented by Dr Friedrich von Wintzingerode, Roche/Genentech
15th May 2018


Challenges In Therapeutic Biological Products

Presented by Paolo Grisostomi, Senior Engineer, Materials Science at Biogen and Donald Young, Sr. Product Manager at Thermo Fisher Scientific and Dr. Sona Kovackova, Study Director Small Volume Parenteral applications, Nelson Labs Europe
18th August 2022


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