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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

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


Livdelzi improves ALP normalisation rates in Phase III PBC study


Camzyos shows sustained benefit through 56 weeks in paediatric obstructive HCM


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Past Webinars

The Paperless Laboratory: A Way Into Process Optimisation

Presented by Peter Boogaard
05th November 2015


Using PAT to accelerate and optimize the process development of solid dosage forms.

Presented by Lizbeth Martinez, Ph. D. Associate Director Data Science, Oral Pharmaceutical Development at Novartis Basel Switzerland and Emiliano Genorini, Account Manager – MicroNIR at Viavi Solutions
04th November 2021


Final Revised Version of BioPhorum Extractable Testing Recommendation Part 2

Presented by Sara Ullsten, R&D Section Manager, Cytiva and Haiyan Hong, R&D manager of Life Sciences at Saint-Gobain
11th June 2020


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