On-Demand Webinars

1. Optimizing The Progression Of Biotherapeutic Candidates To FIH Studies 6/9/2025

   Learn actionable strategies that can lead to higher success rates and smarter resource investment, paving the way for a successful path to IND submissions and commercialization.

2. Simplify CAR-T Cell Manufacturing With LNP-Mediated Delivery 6/3/2025

   Streamline CAR-T cell manufacturing with lipid nanoparticles delivering base editors to create fratricide-resistant, CD45-edited CAR45 T cells, which enables scalable, precise, and potent therapies for blood cancers.

3. A New Look At Subcutaneous mAb Delivery Using Nanoformed Particles 6/3/2025

   A highly concentrated non-aqueous suspension of an IgG1 was developed using a patented platform. Review how the particle size of the monoclonal antibody (mAb) impacts the overall behavior of the drug product.

4. The Advantages Of Off-The-Shelf GMP iPSCs With A DMF 6/2/2025

   Learn how off-the-shelf, GMP-grade iPSC lines with a Drug Master File (DMF) can accelerate cell therapy development, streamline regulatory approval, and reduce time and cost to clinic.

5. Key Bioassay Strategies For Successful IND Submission 6/2/2025

   Watch Erika Kovacs, Senior Director of Bioassay, as she discusses critical considerations for developing stage-appropriate bioassays to support complex biologics and bioconjugates on the path to IND.

6. Advancements In Evaluating Fc-Mediated Functional Activity In Biologics 6/2/2025

   Watch this presentation to gain a comprehensive overview of how to evaluate Fc-mediated functions — and why doing so is vital to the success of biologic therapies.

7. How To Optimize Labeling In A Pharmaceutical Environment 5/29/2025

   Accurate, readable pharmaceutical labels are crucial. Learn to navigate considerations like printing, application tolerances, and inspection to select the right machinery for your production environment.

8. Accelerate And Enhance Biomanufacturing Operator Training 5/28/2025

   Unlock the power of blended operator training and learn how combining digital tools with hands-on instruction reduces errors, boosts retention, and empowers your workforce for real-world production success.

9. Considerations For Tangential Flow Filtration Process Development 5/27/2025

   Optimize your TFF process with single-pass technology by joining experts Mike Dango and Michael Brauchle as they share key strategies for scalable, efficient filtration process development.

10. Navigating Regulatory Shifts: EU GMP Annex 1 And USP 382 5/20/2025

    Strengthen risk mitigation strategies while ensuring regulatory alignment. Gain valuable insights into best practices and proactive approaches for building a robust and future-ready CCS.