On-Demand Webinars

  1. Overview Of FDA's Expedited Program For Serious Conditions 8/15/2025

    Review more details on the FDA expedited review programs, the incentives for obtaining such designations, and the required information/data to better position your investigational product for success.

  2. Addressing Raw Material Handling Challenges By Dry Granulation 8/12/2025

    Handling multi-ton quantities of buffers, salts, and stabilizing chemicals in manufacturing can be difficult. Discover how dry granulation improves efficiency, safety, and process reliability.

  3. How Compliance-Driven CDMOs Win Sponsor Contracts 8/6/2025

    Discover how evolving global regulations are reshaping CDMO strategy. and how digital infrastructure helps manufacturers stay audit-ready, build sponsor trust, and turn compliance into an advantage.

  4. Designing IND-Enabling Toxicity Studies For Complex Drug Modalities 8/6/2025

    Learn more about how we adapt and enhance conventional small molecule IND-enabling studies to align with the evolving demands of modern therapeutics.

  5. Process Intensification: Your Guide To "Doing More With Less" 8/5/2025

    Explore innovative strategies in process intensification to boost mAb production and hear from industry experts as they share solutions for scaling efficiency and navigating regulatory challenges.

  6. Accelerated Tech Transfer With Integrated, Client-Focused Project Management 7/30/2025

    Observe how integrated project management and co-located DS/DP operations streamline technology transfer, reduce risks, and accelerate biopharmaceutical development timelines.

  7. Leverage Process Analytical Technology For Developing Novel Conjugates 7/29/2025

    Explore how Process Analytical Technology accelerates novel conjugate development and how PAT is integrated with an ADC platform to enhance efficiency, data quality, and product consistency.

  8. Sustainability By Design In API Manufacturing 7/29/2025

    Explore the urgent need for sustainability in small molecule API manufacturing, as well as reveal regulatory drivers, green chemistry innovations, and practical strategies to reduce emissions.

  9. Maximizing Results For Viral Clearance Studies 7/25/2025

    Explore virus strain selection and titer strategies to optimize viral clearance studies, covering regulatory expectations, study design, and execution best practices.

  10. Can Your Facility Cleaning, Environmental Monitoring, And Disinfection Process Pass Regulatory Scrutiny? 7/25/2025

    Explore facility cleaning, monitoring, and disinfection strategies to meet regulatory standards, emphasizing planning, stakeholder involvement, testing, trending, documentation, and continuous improvement.