On-Demand Webinars

  1. Introducing 2 New Highly Effective ADC Payloads For Cancer Therapeutics 11/6/2024

    Unlock the potential of antibody-drug conjugates (ADCs) by exploring our novel payloads, designed for easy access and evaluation, to accelerate your ADC drug development with proven efficacy and safety.

  2. From iPSCs To Functional NK Cell Therapy - A Client Journey 10/30/2024

    Discover how iPSC-based allogeneic cell therapies, guided by Cellistic's top experts and powered by Pulse and Echo platforms, are set to transform healthcare.

  3. Regulatory Considerations Including Extractables & Leachables For Single-Use Manufacturing 10/29/2024

    Watch to gain insights into regulatory guidance for single-use manufacturing and risk assessment strategies for single-use implementation.

  4. How To Plan For Trouble-Free Filter Validation 10/28/2024

    Watch to learn when filter validation should be performed, what is required from an end user and laboratory testing perspective, and how to achieve first-time success for various drug products.

  5. Reducing Risks By Outsourcing OSD Manufacturing And Packaging 10/23/2024

    Watch to discover the key benefits of outsourcing your OSD production and explore real-world examples and best practices to help you streamline your processes and enhance your operational agility.

  6. Accelerating Nasal Dosage Form Development From Early-Phase To Clinical Trial Manufacture 10/21/2024

    Led by Dr. Richard Johnson, Chief Scientific Officer, this 40-minute session covers the five key stages of the UpperNose development platform, highlighting the significance of target product selection and its influence on formulation and clinical outcomes.

  7. Use Of Spray Drying In Pharmaceutical Product Development 10/21/2024

    Through this detailed exploration, participants will gain valuable knowledge on how to leverage spray drying to optimize drug development and delivery.

  8. Achieving Manufacturing Efficiency In OSD Manufacturing 10/16/2024

    Gain expert insight into the importance of instrumented tablet presses in assessing formulation properties, the role of tablet cup configurations, and scalability parameters for successful product transfer.

  9. Breaking Barriers: Combining Cell Line Development Innovation With Improved Process Development Workflows To Streamline Path To FIH 10/16/2024

    Explore how KBI Biopharma’s SUREtechnology Platform™, powered by Selexis®, accelerates the development of complex biologics from early stages to first-in-human (FIH) trials, focusing on both speed and quality.

  10. 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.