On-Demand Webinars

  1. Future-Proofing The Material Transfer Process In Your Facility 5/1/2025

    Minimize contamination risks in Grade A/ISO 5 areas. Discover how integrating automated bio-decontamination with manual methods enhances your cell and gene therapy material transfer program.

  2. CLD To Upstream Optimization: Enhancing Biologics Quality, Productivity 4/30/2025

    Explore how advanced cell line development and upstream processing strategies optimize both productivity and therapeutic effectiveness, ensuring the development of high-quality biologics.

  3. 3D Screen Printing: Breakthrough Solutions For Patient-Centric Therapies 4/29/2025

    Explore 3D screen printing’s potential to revolutionize pharmaceutical manufacturing with scalable, customizable, multi-drug tablets and precise, patient-centric drug release profiles.

  4. A Modern Environmental Monitoring System That Grows With Its Tasks 4/24/2025

    Modern environmental monitoring systems are vital for pharmaceutical manufacturing. Explore the benefits of a tool for data collection, analysis, and processing that ensures compliance and adaptability.

  5. Why And Where To Monitor In Aseptic Processing Areas 4/24/2025

    Annex 1 mandates a risk assessment to identify optimal sample point locations. Explore factors in risk assessment, equipment selection, and system design to maximize data value.

  6. Inside The Development Of An AAV8 Production Platform 4/24/2025

    Explore innovative solutions for AAV8 production challenges, which include scalability and purity, as well as learn how a collaboration with CDMO Matica Biotechnology ensures efficient, high-yield gene therapy vector production.

  7. Sustainable Manufacturing Through Efficient BioProduction Unit Operations 4/23/2025

    Delve into the critical environmental and economic aspects of bioprocessing. Explore the urgent need to manage the industry’s growing plastic waste issue and a three-pronged approach to address this challenge.

  8. Spray Dried Dispersions: Performance, Manufacturability, Stability 4/17/2025

    Explore advanced approaches to designing robust amorphous formulations and optimizing spray drying processes tailored specifically to difficult-to-formulate compounds.

  9. Navigating Global Regulatory Landscapes In An Evolving Biopharma Industry 4/15/2025

    Minimize regulatory risks and ensure compliance in the evolving biopharma sector. Watch this on-demand discussion for insights on change management, supplier collaboration, and future market trends.

  10. A Holistic Approach To Process Scale-Up 4/14/2025

    Explore an innovative concept that optimizes USP and DSP processes, as well as discover scale-up results and a fully automated and integrative DSP system.