MilliporeSigma Webinars

1. Practical Applications For Controlled And Safe Nucleic Acid Delivery 7/21/2025

   Explore the science behind LNP formulation development, from ionizable lipids to scalable manufacturing through case studies, screening strategies, and flexible approaches for advancing next-generation therapeutics.

2. 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.

3. An Early Formulation Screening Service 5/23/2024

   Gain insights into overcoming the challenges in lipid nanoparticle (LNP) formulation, explore critical aspects of the process and analytical development of LNPs, and much more.

4. Establishing Analytical Methods For Emerging mRNA-Based Therapies 6/5/2023

   Here, we describe the use of cutting-edge technologies to assess critical quality attributes of both mRNA drug substances and drug products.

5. Plasmid DNA Downstream Purification Process 4/11/2023

   Large scale production of plasmid DNA requires an in-depth understanding and optimization of the entire downstream process. Explore a complete solution, from harvest to bulk filtration.

6. RNA Interference - From Single Gene Studies To Whole Genome Screens 11/7/2022

   Endoribonuclease-prepared siRNAs (esiRNAs) are able to overcome the limitations of RNAi. Learn about esiRNAs, their advantages over standard siRNAs, and ways this technology is utilized in different research fields.

7. Keys To Successful mRNA Manufacturing 4/26/2022

   How can PCR-based technology accelerate mRNA development and manufacturing and design principles/critical parameters to enable the rapid development of lipids for RNA formulation?

8. Effective, Efficient Downstream Purification For Plasmid DNA 4/26/2022

   Learn about a complete purification process flow that overcomes the challenges of producing pDNA – a critical first step in mRNA manufacturing – and covers all downstream unit operations.

9. Regulatory Guidance For Bioprocessing Software 2/9/2022

   Gain an understanding of the regulatory requirements for software in a biopharmaceutical GxP environment and how software is invaluable for creating an audit trail, reporting, and automating regulatory-related tasks.

    

10. Frontiers In Digital Bioprocessing 2/8/2022

    In this talk we will dive into 2 digital technologies: modular design and cloud. Both areas have the potential to accelerate the critical aspects of the facility of the future.