MilliporeSigma Webinars
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How To Boost AAV Titer With Feed Supplementation In Both HEK293 And Sf-9 Platforms
11/25/2024
Explore how optimizing post-transfection or post-infection feeding in HEK293 and Sf-9 cells significantly boosts AAV titers, enhancing production efficiency for gene therapy applications.
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Integrating CPV And APQR Data And Workflows To Reduce Redundant Activities
11/15/2024
Experts in the pharmaceutical industry share insights on how to effectively implement a strong, integrated CPV and APQR framework. Watch now and learn how automation enhances efficiency.
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The Road To Approval: Viral Clearance Strategies For Non-Enveloped Viral Vectors
10/10/2024
Know the differences between designing a viral clearance study for non-enveloped viral vectors versus those for mAbs or recombinant proteins, and learn how to identify and remove viral contaminants.
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What Do You Need To Qualify A Single-Use Assembly?
10/2/2024
Explore best practices for the qualification of single-use systems, focusing on quality and regulatory documentation.
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Virus Filtration In Continuous Processing: Novel Approaches For Optimal Performance
9/23/2024
Watch to explore two novel approaches that have been developed to overcome the limitation of a filter's viral retention performance in continuous processes.
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Process Intensification Of Monoclonal Antibody Purification Process
9/23/2024
Watch to explore an intensified mAb purification process that utilizes leading purification technologies, highlighting intensified capture, polishing, and drug delivery.
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Collaborative Bioprocessing: Next-Gen mAb Downstream Manufacturing
9/23/2024
Explore the bioprocessing template, operational paradigm, and the complexities of qualifying an advanced, highly automated bioprocessing train designed for the production of mAbs and other biologics.
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What Do You Need To Do To Qualify A Single-Use Assembly?
8/28/2024
Learn about the implementation of single-use technologies, single-use user requirement specifications, and best practices for single-use qualification, including quality and regulatory documentation.
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Navigating Cleanroom Compliance For Safe Material Transfer
7/23/2024
Watch to explore various aspects of environmental monitoring essential for the transfer of materials into controlled areas as well as recent advancements that can facilitate this task.
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Make More Lentivirus And Make It Right The First Time
6/14/2024
Discover how you can achieve higher titers and robust yield with an optimized, end-to-end lentivirus platform, designed to maximize production and quality for the success of your cell or gene therapy.