MilliporeSigma Webinars

1. Managing Nitrite Impurities: Supplier-Manufacturer View 12/19/2024

   Examine nitrites in excipients, nitrosamine risks, regulatory considerations, analytical controls, and a case study on mitigating risks in pharmaceutical manufacturing and storage.

2. Demonstrating Technical Excellence In Contract Manufacturing 12/10/2024

   Tech Talks explore ADC development innovations, including integrated supply chains, seamless pilot-to-GMP scale-ups, and advanced process analytical technology (PAT).

3. 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.

4. 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.

5. 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.

6. 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.

7. 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.

8. 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.

9. 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.

10. 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.