Key Sessions
Kristy Wood
Leveraging Gene Editing Technologies for Precision and Efficiency in Cell and Gene Therapy Development
Intellia Therapeutics
Ying Cai
Keynote Panel Discussion: Strategies for Scaling Up, Accelerating and Commercializing Gene Therapy Manufacturing
Ultragenyx Pharmaceutical
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Wednesday, September 17th, 2025 - Main Conference Day One - ET (Eastern Time, GMT-05:00)
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Wednesday, September 17th, 2025 - Main Conference Day One - ET (Eastern Time, GMT-05:00)
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Gene Therapy Manufacturing & Analytics
8:50am - 9:00am
Chairperson’s Opening Remarks: Gene Therapy Manufacturing & Analytics
- Francesca Vitelli, PhD - VP Global head of Process and Analytical Development and Innovation (PADI), Minaris
9:00am - 10:00am
Keynote Panel Discussion: Strategies for Scaling Up, Accelerating and Commercializing Gene Therapy Manufacturing
- Ying Cai - MSAT Executive Director, Ultragenyx Pharmaceutical
- Nripen Singh - Head of Process Development, TRD CGT, Novartis
- Vaishali Shukla - Vice President, CGT & API Global Expansion, Eli Lilly and Company
- James Warren - Senior VP, Global CMC Development, Ultragenyx Pharmaceutical Inc.
10:00am - 10:30am
Tech Transfer Best Practices in Gene Therapy
- Jordan Ball - Sr. Manager, Technology Transfer, Regeneron
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Gene Therapy Manufacturing & Analytics
11:30am - 12:00pm
Expanding the Upstream Toolbox: Enabling High-Productivity, Robust, and Scalable AAV Production
- Huize Yan - Senior Scientist, Cell Culture Development, Genentech
12:00pm - 12:30pm
Rapid Development of AAV Purification Process Without Sacrificing Recovery
- Hunter Reese - Scientist II, AskBio
12:30pm - 1:00pm
Accelerated Downstream Development of Viral Vectors Using High-Throughput Process, Analytical, and Formulation Technologies
- Kevin Vera - Scientist II, Process Development, Pharma Services Group, Thermo Fisher Scientific
- Junyan Zhang - Sr Manager, Downstream Process Development, Pharma Services Group, Thermo Fisher Scientific
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Gene Therapy Manufacturing & Analytics
2:10pm - 2:15pm
Chairperson’s Opening Remarks: Gene Therapy Manufacturing & Analytics
- David Dobnik - Research Councillor, National Institute of Biology
2:45pm - 3:15pm
Application of Novel Technologies to Deliver AAV Downstream Processes with Higher Yield and Better Quality
- Junfen Ma - Head of Genomic Medicine Purification Process Development, Sanofi
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Gene Therapy Manufacturing & Analytics
4:30pm - 5:00pm
Detectability and Propagation of MVM in HEK293 Cells: What it means for your Viral Safety Strategy
- Dana Schreffler - Sr. Manager QC Viral Safety, Regeneron
5:00pm - 5:30pm
Mastering hcDNA: A Harmonized CMC Approach in AAV Therapies
- Parag Kumthekar - Gene Therapy Downstream Process Development Lead, UCB Pharma
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