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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

Enabling Total Biopharma Solutions

Pall Life Sciences

Best Practices For Successful Filter Integrity Testing Using Water Intrusion Test (WIT) Method

Monica Cardona and Ian Johnson Pall Life Sciences

Beyond Quality: PAT as a Catalyst for Carbon Reduction in Pharma

Continuous processing optimization with smarter tools

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

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Headline News

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


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


Lilly highlights retatrutide, Taltz and Zepbound data across rheumatologic diseases and obesity


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Upcoming Webinars

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Past Webinars

Modernizing Biopharmaceutical Manufacturing: from Batch to Continuous Production

Presented by Robert Dream, PE, CPIP, of HDR Company, LLC
19th July 2017


Addressing Material Properties in the Design of a Direct Compression Continuous Manufacturing System

Presented by Professor Fernando Muzzio, Professor II in the Department of Chemical and Biochemical Engineering at Rutgers
16th January 2014


Current USP Perspectives on a Rapid Sterility Test

Presented by Presented by Dr David Roesti, Novartis/USP and Erin Patton, Senior Product Specialist, Charles River
30th May 2018


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