MilliporeSigma Webinars

  1. Regulatory Considerations Including Extractables & Leachables For Single-Use Manufacturing 10/29/2024

    Watch to gain insights into regulatory guidance for single-use manufacturing and risk assessment strategies for single-use implementation.

  2. Full Speed Ahead: Accelerating Your CHO Bulk Harvest Testing Using Rapid Methods 10/3/2024

    With advanced rapid methods that offer both speed and sensitivity, you can expedite your bulk harvest testing and detect adventitious viruses in half the time compared to conventional techniques.

  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. 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.

  8. PAT Implementation For ADC And Bioconjugation Processes 3/1/2024

    Explore expert insights into the implementation of Process Analytical Technology (PAT) for ADC and bioconjugation processes and the pros and cons of in(on)line testing for the conjugation process.

  9. Advancements In Process And Payload Development 2/29/2024

    Continuous advancements in the process and payload development of ADCs and next-generation bioconjugates have the potential to progress targeted therapeutics and improve patient treatment options.

  10. The Closed Processing Advantage: Optimizing Biopharma Facilities 11/16/2023

    Explore the evolving landscape of biopharma facility design and operations, including key market trends, closed processing benefits, and industry efforts to harmonize guidance and best practices.