Cell And Gene Therapy Manufacturing
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BPI Interviews Purification And Pharma Analytics Leader
6/9/2025
Jean Luo, VP of Purification and Pharma Analytics, discusses innovations in bioprocessing, including the development of dPCR assays, lentiviral titer systems, chromatography resins, and supply chain.
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HyPerforma 5:1 Single-Use Bioreactor (S.U.B.) Setup And Installation Part 3
5/7/2020
This video is part 3 of 3 videos that cover setup and installation topics related to the HyPerforma 5:1 Single-Use Bioreactor, or S.U.B. In this video we will cover probe assembly, making CPC AseptiQuik connections, probe insertion.
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How Past Gene Therapy Approvals Are Shaping the Future with Dr. Peter Marks
1/30/2024
In this segment of Cell & Gene Live, Dr. Peter Marks shared what he and his team have learned from current gene therapy approvals to accelerate future approvals.
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Scaling Plasmid DNA Production: A Proven Strategy For Higher Yields
8/27/2025
Learn how an agile manufacturing partner scaled their plasmid DNA production and achieved higher yields by optimizing their media selection and fermentation processes.
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Considerations For Affinity Capture In An AAV Platform Downstream Process
6/2/2025
This presentation explores the considerations when evaluating a platform affinity capture step for the purification of AAV vectors. Specificity, binding capacity, purity, yield, scalability and reusability are parameters that will be addressed.
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Optimization Of Anion Exchange Purification For The Large-Scale Production Of Plasmid DNA
11/4/2025
In this webinar, we discuss pDNA purification, including how to identify optimal conditions for various chromatography media and optimize recovery and impurity removal.
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Enhancing AAV Purification In Gene Therapy Manufacturing
6/2/2025
Review chromatography solutions for purifying multiple AAV serotypes, with specialists’ insights on bioprocessing and downstream optimization.
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mRNA For Cancer Immunotherapy 2024 Outlook | Audience Q&A
1/29/2024
During our Cell & Gene Live, mRNA For Cancer Immunotherapy 2024 Outlook, our expert panelists answered audience questions regarding patient safety, foreseeable challenges in mRNA cancer immunotherapy for solid tumors, and much more.
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Focal Points for 2024: Dr. Verdun and Dr. Marks Talk Regulatory Challenges for Cell-Based Therapies
1/30/2024
Dr. Verdun and Dr. Marks provide detailed feedback on the regulatory challenges facing cell therapy and explain the Agency’s most important focal points for 2024, patient accessibility, and more.
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Quality Roundtable: Optimizing Biologics Manufacturing Processes With Raw Materials
1/24/2024
Improve your commercial manufacturing process with advice from regulatory and raw materials experts on the development journey from pre-clinical to licensure.