Insights On Facility Design

  1. Mastering Pharmaceutical Cleaning Validation Methods 6/22/2026

    View the basics of cleaning validation and discuss the support services you should seek from your critical cleaning products supplier to optimize your cleaning validation process.

  2. Better, Safer Science Through Proper Detergent Selection And Cleaning 6/22/2026

    Enforce reliable lab results by improving washer performance, detergent selection, and rinsing to prevent residues, cross-contamination, and spotting—supporting reproducibility and compliance.

  3. 5 Common Pitfalls In CGT Facility Design Planning And Implementation 6/15/2026

    With shifting needs and requirements in advanced therapy manufacturing, embedding infrastructure flexibility is vital. Discover how to balance these variables for long-term success.

  4. Why Cost-Sensitive Innovation Is Underrated In Development 6/12/2026

    Gain insight into how strategic decisions around equipment are enabling teams to manage complexity, improve scalability, and advance therapies without compromising financial sustainability.

  5. How Equipment Choices Can Help Determine The Pace Of Drug Development 6/12/2026

    The speed of drug development depends as much on equipment choices as scientific expertise. See how flexible, integrated tools reduce delays, improve data quality, and enable faster decisions.

  6. New Robot-Compatible Sterile Connectors Enhance Cell Therapy Manufacturing 6/11/2026

    Discover how automating sterile fluid transfers removes human contamination risks, solves operator shortages, and reduces cell therapy manufacturing costs by up to 74%.

  7. Improve Process Control And Achieve More Consistent Outcomes 6/4/2026

    Mixing efficiency at scale depends on more than speed alone. Gain insight into data that reveals how fill levels and vortex formation impact homogenization time, offering practical guidance.

  8. Advancing Through A Single-Use Facility Journey 5/28/2026

    Modular single-use facility design — combining closed processing and global standards — boosts flexibility, speeds tech transfer, and strengthens supply resilience in modern biomanufacturing networks.

  9. Best Practices For Building A Multi-Product Manufacturing 5/27/2026

    Multi-product ATMP facilities need integrated teams, flexible design, and strategic HVAC to ensure scalability, contamination control, cost efficiency, and reliable long-term performance.

  10. The Framework For Containment In A Cleanroom 5/20/2026

    ISO classification decisions shape cleanroom design. Learn how early alignment between process needs, biosafety, and classification can reduce redesign risk while supporting scalable environments.