On-Demand Webinars

  1. How To Get Regulated Products To Market Faster With A Composable MES 1/21/2026

    See how a medical device manufacturer launched a fully digital, paperless factory in nine months. Explore strategies for scaling, validation, and operator engagement using gamification and AI.

  2. T3P – A Green Solution For Peptide Coupling, Water Removal Reactions 1/13/2026

    The session focuses on the use of T3P (propanephosphonic acid anhydride) in amidation and peptide coupling reactions, including both liquid-phase and solid-phase peptide synthesis.

  3. Reimagining API Manufacturing – How To Achieve Smarter, Scalable Flow Chemistry 1/13/2026

    Designed for scientists and engineers evaluating advanced reactors, this recording delivers practical insights and real-world examples to support safer, more efficient, and adaptable flow chemistry.

  4. Compliance In Conversation: A Fill And Finish Regulatory Roundtable 1/7/2026

    Explore Annex 1 expectations, PFAS legislation, and contamination control strategies in this expert-led discussion, as well as practical insights on risk mitigation, validation, and inspection readiness.

  5. Boost Process Efficiency With Our New mAb Optimized TFF Cassette 1/7/2026

    Discover how optimized membranes and screen designs enable higher mAb concentrations, improved flux performance, and scalability, while addressing TFF process challenges.

  6. Enhancing Automated Environmental Monitoring In Gloveless Isolators 1/7/2026

    Explore how automation and robotic-friendly solutions are transforming fill-and-finish operations and gain insights into gloveless processes, EM testing challenges, and collaborative innovations.

  7. The Impact Of PEGs In The Small Molecule API Market 12/22/2025

    Explore how PEG selection shapes drug development success by understanding the benefits of expert CDMO partnerships that deliver custom solutions to enhance your small molecule program.

  8. Five Practical Considerations To Move From Concept To Clinic 12/17/2025

    Learn more about five key factors for advancing targeted in vivo LNP programs, from formulation and targeting strategies to bioanalytical readiness and scalability.

  9. Agile Adaptation In mRNA-LNP Manufacturing: A CDMO's Response 12/17/2025

    Find flexible scale-up from lab through commercial manufacturing, leveraging expertise. Gain technical insights for scalable, efficient development for advancing mRNA, saRNA, or circular RNA programs.

  10. Bridging The Gap Between Product Readiness And Equipment Availability 12/15/2025

    Discover how manual precision at scale bridges packaging gaps, accelerates product launches, and ensures uninterrupted supply to deliver quality when automated equipment isn’t yet operational.