pharm-stream-recent-webinars

1. March Cytiva Webinar 3/11/2026
2. 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.

3. 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.

4. 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.

5. 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.

6. 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.

7. 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.

8. 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.

9. 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.

10. Extrusion-Based ASD Scale-Up: Performance Through Process Understanding 11/20/2025

    Explore the formulation and manufacturing considerations for amorphous solid dispersions (ASDs), with a focus on hot melt extrusion (HME) as a scalable and cost-effective technology option.