MilliporeSigma Webinars

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. Filling The Sterility Testing Gap: Traceability And 21 CFR Part 11 Compliance 6/6/2024

    Watch to learn about a solution that offers digital information for every stage of a sterility test while remaining compliant with 21 CFR Part 11.

  10. Unleashing The Power Of Perfusion In Intensified Processes 5/28/2024

    Explore the advantages of implementing a perfusion-specific CLD process to produce more productive clones as well as an integrated solution for intensified processing.