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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

Pasritamig combination delivers 73% PSA response rate in advanced prostate cancer Phase I study


Onchilles reports early systemic activity with intratumoral N17350 in Phase I/II trial


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


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Past Webinars

Single Use Manufacturing within the Bristol-Myers Squibb Manufacturing Network – Preparing for Commercial Production

Presented by Lance Marquardt, Associate Director - Upstream Processing for Hopewell Clinical Manufacturing at Bristol-Myers Squibb and  Sara Bell, Senior Marketing Manager for Merck’s single-use product portfolio
17th January 2019


Advances in the Purification of Antisense Oligonucleotides

Presented by Robert Gronke, Ph.D., Senior Principal Scientist, Technical Development, Biogen and John Cyganowski, Director of Customer Application, Downstream, Merck
27th October 2021


Mixed mode Chromatography in Purifying biologics – Overview

Presented by Vivek Halan, Senior Scientific manager at Zumutor Biologics Pvt Ltd
15th November 2018


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