Facility Design Webinars
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Aseptic Filling Quality Through Assurance
3/20/2026
Meet the quality specialist who ensures every workcell is built correctly and ready for therapeutic production. His detailed final checks help confirm each system performs reliably before it leaves.
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Aseptic Filling Quality With A Sense Of Pride
3/20/2026
Skilled polishing sets the foundation for aseptic manufacturing. Meet the team refining stainless steel components with precision and consistency to ensure surfaces can be effectively decontaminated.
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Trends In Mid-Size Scale Up Strategies
3/13/2026
A development leader highlights supply‑chain resilience, cost‑efficient large‑scale manufacturing, proven tech‑transfer success, and long‑term commitment to supporting clients through reliable scale‑up and global production strategies.
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Practical Considerations For Aseptic Gowning In Contamination Control Strategies
2/26/2026
Master the complexities of aseptic gowning and Annex 1 compliance. Explore risk-based strategies to mitigate human-source contamination and strengthen your facility's sterility assurance.
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Regulatory Compliance And Advanced Solutions For Aseptic Environmental Monitoring
1/29/2026
Modern aseptic monitoring requires a shift from periodic checks to risk-based strategies. Learn how to integrate particle and environmental data to meet Annex 1 standards and ensure patient safety.
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Building Digitally Connected Packaging Operations With Open Standards
1/29/2026
Connect shopfloor equipment with enterprise systems to streamline your data flow. Learn how automation standards enhance integration and see a live demonstration of unified line performance in action.
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Putting Pressure On CDMOs With Herman Bozenhardt
1/27/2026
In this episode of “Better Biopharma,” host Tyler Menichiello is joined by Herman Bozenhardt, a consultant and industry veteran who has spent decades advancing the fields of biopharmaceutical manufacturing, engineering, and regulatory compliance.
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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.
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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.
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Streamlining pDNA: Capacity, Complexity, And Cutting-Edge Solutions
11/20/2025
Learn how flexible facility design and process innovation are accelerating pDNA manufacturing, as well as key strategies to avoid scale-up pitfalls and meet growing therapeutic demand.