On-Demand Webinars

  1. Next-Generation Digital Technology For Pharma R&D And Manufacturing 2/27/2025

    The panel explores what the next generation of digital technology will look and feel like from users’ perspective. Hear from experts at Microsoft, GSK, TetraScience, Emerson and IDBS.

  2. Monitoring Compressed Gases For Microbial And Particle Contamination 2/26/2025

    There are several factors associated with active environmental microbial monitoring. Watch to learn how the EU GMP Annex 1 compliance focuses on microbial monitoring in cleanrooms.

  3. Understanding ISO/TR 14644-21 Airborne Particle Sampling Techniques 2/26/2025

    Industry expert Mark Hallworth guides viewers through the latest ISO document (ISO 14644), exploring the reasons behind the decisions made by the team during its development.

  4. Digital Enhancements For Operational Excellence 2/20/2025

    Unlock operational excellence with digital enhancements. Discover practical strategies to reduce errors, streamline processes, and drive continuous improvement across industries.

  5. Mastering QbD For Successful Process Validation Campaigns And Commercial Manufacturing Of Biologics 2/18/2025

    In this presentation, industry-leading bioprocess experts explore the challenges and opportunities that arise when implementing Quality by Design (QbD) in biologics development and manufacturing.

  6. Efficient Downstream Processing Of Antibody-Based Therapeutics – A CDMO Perspective 2/18/2025

    Discover efficient downstream processing strategies for antibody-based therapeutics. Explore key considerations and trade-offs in purity, yield, speed, and cost, from a CDMO perspective.

  7. Contract Manufacturing: Must-Know Trends And Strategies For 2025 2/12/2025

    Regulated industries face rising demand, tech breakthroughs, and regulatory harmonization. Discover how contract manufacturers must leverage AI and cloud solutions to stay agile and compliant in the future.

  8. Essential Considerations For Selecting The Right Biologic Fill/Finish Partner 2/12/2025

    Partnering with a provider that prioritizes quality and yield optimization not only ensures product safety but also helps reduce operational costs.

  9. Purity As A Priority: Optimizing Safety Measures For rAAV Therapies 2/11/2025

    Watch to learn how rAAV vectors in gene therapy are addressing manufacturing impurities, risks to patient safety, and analytical methods for detection while aiding sponsors in regulatory compliance.

  10. LBA Vs. LC-MS: Competing Technologies At A Development Crossroad 2/6/2025

    Watch as bioanalytical experts Shane Karnik, MS, and Matt Hartle, Ph.D., explore why many sponsors are reevaluating the use of LBA for large molecule protein analysis in favor of LC-MS.