On-Demand Webinars

  1. Compliance To Confidence: Annex 1 For Small-Batch, High-Value Production 10/3/2025

    Get strategies for meeting the updated GMP Annex 1 in small-batch aseptic filling. Learn about contamination control, quality management, and equipment design for high-value liquid and powder products.

  2. Liquid Phase Peptide Synthesis: Regulatory, Analytical, And QC Perspectives 10/3/2025

    Discover how Liquid Phase Peptide Synthesis (LPPS) uses traditional reactors to create more efficient and sustainable peptide manufacturing. Learn about key analytical and quality control considerations.

  3. Complex Antibody Expression - Challenge Accepted 10/2/2025

    Explore how tailored cell line development strategies are enabling high-yield production of complex biologics and reveal how automation and data modeling drive success in CHO cell line development.

  4. Supply Resiliency For Bioprocessing Amid Global Volatility 10/2/2025

    Build bioprocessing resiliency with strategic supply chain management. Learn to meet quality, compliance, and time-to-market demands amid global volatility with effective sourcing.

  5. Process Intensification Strategies For Smarter Biomanufacturing 10/1/2025

    Explore how biopharma leaders are using process intensification to modernize facilities, cut costs, and increase yield with practical strategies and real-world case studies.

  6. Automated Immunoassay For AAV Capsid Titer Measurement 9/30/2025

    Explore how automated immunoassays outperform ELISA in AAV quantitation—offering better sensitivity, precision, and matrix interference management to help you identify the best media for high viral titers.

  7. Accelerate Analysis Of Titer, Process Impurities, And Process Contaminants 9/30/2025

    Learn how automated immunoassay platforms can accelerate titer and impurity analysis in AAV and LV vector workflows—reducing hands-on time while improving consistency from development through manufacturing.

  8. Rethinking MES In Pharma: Faster Reviews, Better Data, Less Risk 9/30/2025

    Discover how composable MES helps pharma teams scale faster, enforce SOPs, and maintain data integrity—while empowering frontline teams to build workflows that fit their operations.

  9. Utilizing Flow Cytometry For Humoral Immunogenicity Testing: Cell & Gene Therapy 9/29/2025

    Discover strategies to overcome immunogenicity challenges in cell and gene therapies, with a focus on harnessing flow cytometry to enhance ADA and NAb assay development, strengthen validation, and ensure regulatory readiness.

  10. Optimizing Aseptic Processing With Isolator Technology 9/29/2025

    Discover how pharmaceutical isolators optimize operations, achieve higher sterility assurance, and meet stringent regulatory requirements. Learn about design principles, validation, and VHP cycles.