Enterprise Solutions Webinars

  1. PUPSIT Without The Pain: Practical Solutions For Implementation 5/6/2025

    Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as learn about integrity testing, wetting procedures, and innovative filtration systems for effective implementation.

  2. Accelerate Development With Excipient GMP Quality Cell Culture Solutions 4/21/2025

    Reduce risk and speed up timelines as you move towards commercialization. Learn about end-to-end services offering Excipient GMP cell culture solutions for streamlined development and regulatory success.

  3. Innovations In Sterile Connectors Transform CGT Bioprocessing 4/21/2025

    Explore advancements in single-use sterile connectors transforming CGT bioprocessing by enhancing fluid handling, reducing contamination, and improving process reliability for next-gen therapies.

  4. Sterile Gas Filtration And Optimization In Bioprocessing 4/17/2025

    Unlock insights into sterile gas filtration challenges in bioprocessing. Watch this on-demand session to learn optimization strategies for critical applications and improved filter performance.

  5. Reimagine Sustainability In Bioprocessing 4/16/2025

    Achieving sustainability in bioprocessing labs presents distinct challenges. Learn how to reduce your environmental footprint while maintaining efficiency and avoiding extensive re-validation efforts.

  6. Transforming Rare Disease Drug Development For A Faster Cure 4/15/2025

    This comprehensive exploration aims to shed light on the critical aspects of expediting curative therapies, with a focus on the strategic role that CDMOs can play in this transformative journey.

  7. From 10 Days To 3: Transforming ADC Processes With Single-Use Tools 4/4/2025

    Learn how a collaborative partnership streamlined antibody-drug conjugate processes using a single-use, multi-step system to reduce operator time by 68%.

  8. Minimizing Risk In RNA-LNP Encapsulation And Drug Product Manufacturing 3/31/2025

    Learn about an integrated drug substance/drug product offering for your IND program and beyond, with a holistic approach to ensure process robustness at every stage.

  9. Case Study: Purification Solutions For Resilience CDMO 3/31/2025

    Ensuring consistent, high-quality biopharmaceutical production hinges on dependable partnerships. Explore how a collaboration addressed supply chain vulnerabilities, facilitating rapid access to advanced resin technology.

  10. 10 Minutes On Optimizing Upstream Process Development 3/25/2025

    Gain insight into how UPD ensures scalable and compliant processes, facilitates the efficient development of innovative therapeutics, and contributes to molecule development and production.