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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

Health Canada authorizes Moderna’s mRNA flu and combination flu-COVID vaccines


Moderna advances Bundibugyo ebolavirus vaccine toward Phase II/III study


Teva discontinues Phase II emrusolmin trial in multiple system atrophy after futility analysis


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Past Webinars

Material Understanding for Continuous Manufacturing of Solid Dosage Forms

Presented by Dr Yifan Wang, Regulatory Research Scientist, FDA CDER and Dirk Leister, Leader Technical Marketing Thermo Fisher Scientific
23rd August 2018


Sterile Products Manufacturing – prepared for the future?

Presented by Gert Moelgaard
15th February 2018


Extractables and Leachables Testing Using a Quality Risk Management Approach

Presented by Dhaval Tapiawala, Principal Scientist at Pfizer and Dr. Dennis Jenke, Principal Consultant for Nelson Labs
09th September 2020


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