On-Demand Webinars

  1. Manufacturing Made More Robust And Customer-Centric 12/11/2025

    Discover how regional manufacturing, risk-aware practices, and agile strategies are reshaping supply chains to deliver resilience, transparency, and sustainability in today’s complex global environment.

  2. Automating Visual Inspection Qualification 12/11/2025

    Transferring visual inspection data from paper to digital is essential for Pharma 4.0 compliance. Learn practical strategies to eliminate errors, automate data tracking, and enhance quality assurance.

  3. When A Logbook Project Becomes A Digital Movement 12/11/2025

    A leading pharma company accelerated execution and compliance in GMP operations. See how modular apps replaced manual processes, setting a new foundation for continuous innovation.

  4. Lessons From FDA 483s And Warning Letters: Cleanroom Compliance 12/8/2025

    Learn critical lessons from FDA 483 observations and Warning Letters to proactively address common GMP cleanroom compliance failures and build an inspection-ready facility.

  5. Eliminate Risk From Your Viral Vector Tech Transfers 12/5/2025

    Explore strategies to simplify viral vector tech transfers, reduce risk, and maintain quality under tight timelines, as well as a case study that demonstrates how to streamline this critical process.

  6. Navigating Regulatory Expectations For Injectable Packaging 12/4/2025

    Explore insights on extractables, focusing on how they relate to the revised EU GMP Annex 1, new and evolved expectations under USP <382>, and the use of VHP decontamination in aseptic environments.

  7. Cleanroom Changes In 2026 For Better Contamination Control 12/3/2025

    Proactively improve your cleanroom strategy for 2026. Gain actionable insights on leveraging Environmental Monitoring data, optimizing personnel, and managing residue to enhance contamination control.

  8. Optimizing Monitoring: The Science Of Particle Loss 11/26/2025

    Explore how tubing configuration impacts particle recovery and compliance under Annex 1, using evidence-based guidance, risk assessment tools, and practical strategies to strengthen contamination control.

  9. Class 3 Atropisomers: Capture Therapeutic Selectivity In Oncology 11/26/2025

    Atropisomers are key to modern small molecule drug development. Learn how advanced manufacturing strategies enable the isolation and scalable production of the most effective single isomer.

  10. mAb Purification: A Two-Step Approach Using A Strong AEX-HIC Mixed-Mode Resin 11/24/2025

    Elevate your mAb purification with a two-step chromatography strategy. Simplify the process, eliminate an entire step, and achieve substantial savings in time and material costs.