On-Demand Webinars

  1. Leveraging Platform Processes For Developing And Accelerating Novel Gene And Cancer Therapeutics 12/5/2024

    Explore how platform processes advance gene therapies, the impact of strong partnerships on patient access, and the future shaped by these collaborations.

  2. Removing The Headache: Outsourced Stability Storage And Testing Solutions 12/4/2024

    Darryl Souness, Head of Analytical at Cambrex Edinburgh, and Stephen Delaney, Managing Director at Q1 Scientific (a Cambrex Company), share insights on the benefits of outsourcing stability storage and testing.

  3. Charting A Successful CMC Journey For Your ADC Drug Product 12/3/2024

    Learn about best practices and strategies to optimize bioconjugate drug product tech transfers and supplies in clinical or commercial phase, and explore real-world case studies.

  4. Early Preclinical Development: A Successful Transition To cGMP Manufacturing 12/2/2024

    Explore the development steps that lead to an mRNA construct optimized for your requirements and that meets future-proof cGMP manufacturing requirements, thereby de-risking the development.

  5. 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.

  6. Plasmid DNA For Cell & Gene Therapy: It All Starts Here 11/25/2024

    Explore how tailored manufacturing solutions can enhance program outcomes, leverage cutting-edge technologies for research and discovery, and optimize preclinical applications.

  7. Manufacturing Strategies And Facility Design For Patient-Centric Delivery 11/21/2024

    Review how to select the optimal manufacturing strategy and leverage technologies for efficient and scalable production of therapeutic proteins. De-risk the supply chain, accelerate time to market, and reduce costs.

  8. All Biopharma Roads Begin With Eco-Design: How Can You Get Started? 11/20/2024

    Listen to a discussion between Ryan Walker, Cytiva, and Aude Arkam, Sanofi, to learn how the influence of eco-design can guide sustainability in the biopharma industry.

  9. Scope 3 Emissions: Cut The Complexity With Creative Collaboration 11/20/2024

    Delve into the crucial role of Scope 3 emissions in the biopharma industry's sustainability journey, and learn more about the challenges and opportunities of managing these types of emissions.

  10. Using An Adherent Platform To Scale-Up An Upstream Viral Vector Process 11/20/2024

    Gain insight into a helper-dependent adenovirus (HDAd) process that covers everything from bench-scale and optimization to tech transfer.