Upcoming Webinars
Quality by Design: Enhancing Biopharma Validation and Microbial Retention Assurance in Sterilizing Filters
Presented by Gregory S. Blank, Ph.D. Independent Consultant and retired Director, Late Stage Purification Department at Roche Genentech, Annie Leahy, Senior MSAT Manager at MilliporeSigma, Jennifer Juneau, Senior Principal Scientist at Pfizer,
11th June 2025
Big Data Strategies for Cell Therapy Manufacturing
Presented by Scott R. Burger, MD, Principal of Advanced Cell & Gene Therapy, LLC
18th June 2025
Read Across Assessment for Potential Leachables Without Toxicological Data
Presented by Yana Chervona, Drug Safety Team Lead in Drug Safety Research and Development at Pfizer
13th August 2025
Assessing the Use of Solid-Phase Cytometry for Rapid Bioburden Testing
Presented by Sophie Drinkwater, Associate Director in Microbiology at AstraZeneca
19th August 2025
On Demand Webinars
Charting the Universe of Organic Extractables
Presented by Dennis Jenke, Principal Consultant of Nelson Labs EU
12th May 2025
Beyond USP <86>: Supplemental Testing
Presented by Karen Zink McCullough, Owner, Principal Consultant at MMI Associates, John Duguid, Executive Director, Research & Development at Vericel Corporation, Steven Walfish, Principal Consultant at Statistical Outsourcing Services
28th April 2025
Advancing Biomanufacturing Quality Control with GMP Next Generation Sequencing (NGS): Regulatory Insights and Industry Case Study
Presented by Amina Cherif Louazani, PhD, Viral safety and Regulatory affairs Manager at PathoQuest and Dave Briggs, Ph.D., Principal Scientist, Late Stage/Commercial at Avid Bioservices
22nd April 2025
Using Risk Management to Design Aseptic Process Simulations
Presented by Presented by Alberto Gonzalez, Global Sterility Assurance and Microbiology Associate Director at Takeda
16th April 2025
