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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


Featured Articles

Expanding Adoption of Single-Use Systems Drives Need for Wider Range of Sterile Connector Technologies

James Barry, Director of Marketing, Americas, Pall Biotech

Enabling Total Biopharma Solutions

Pall Life Sciences

Continuous processing optimization with smarter tools

Barbara Paldus, Ph.D.
Vice President & General Manager Finesse, part of Thermo Fisher Scientific

Successful Wetting for Filter Integrity Testing in Volume-Restricted Systems

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Headline News

CAPLYTA shows rapid improvement in bipolar mania in second pivotal Phase III study


Zura Bio discontinues tibulizumab development in hidradenitis suppurativa after Phase II miss


FDA grants Priority Review to BRUKINSA combination in first-line mantle cell lymphoma


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Past Webinars

New Drying Processes for Biopharmaceuticals

Presented by Sune Klint Andersen, Principal Scientist at Janssen Pharmaceutical Companies of Johnson & Johnson and Lars Markwort co-founder and CEO of Bioinicia SL
05th May 2020


Towards a lean Manufacturing: Implementing Single-Use Process Analytical Technologies (PAT) tools at the seed stage to simplify cell culture operations

Presented by Dr Jose R. Vallejos of Medimmune/AstraZeneca
24th May 2017


The Business Benefits of PAT in Continuous Drug Product Manufacturing

Presented by Steve Hammond, Independent Consultant at Steve Hammond Consulting
22nd September 2021


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