From bench to batch: Building reproducible cell and gene therapy workflows with GMP-ready reagents

BlueskyReddit
Webinar Date: September 23, 2026
Time: 11:00 AM EDT
Duration: 1 hour
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Lot-to-lot variability in cytokines and growth factors is a persistent cost and scale-up challenge in cell and gene therapy manufacturing — inconsistent raw materials can undermine process reproducibility long before a product reaches the clinic. Join this webinar for a look at how animal origin-free (AOF) recombinant cytokines and growth factors are being formulated to address these variability and documentation gaps.

The session will cover lot-to-lot reproducibility data, bioactivity and protein recovery testing, and the regulatory documentation needed to support both research and GMP-compliant workflows. We'll also discuss how closed-system compatible formats factor into process development and scale-up planning for clinical and commercial manufacturing.

Key Takeaways: 

  • Achieve consistent cell culture with recombinant, animal origin-free (AOF) cytokines and growth factors
  • Ensure performance with guaranteed bioactivity and protein recovery
  • Simplify workflows with plug-and-play reagents and regulatory-ready documentation
  • Support GMP compliance with manufacturing-ready reagents
  • Streamline scale-up with closed-system compatible formats that can reduce cleanroom requirements

Who should attend: 

  • T cell biologists
  • CAR-T manufacturers 
  • Process Development Scientists 
  • MSAT

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Senior Product Manager
Qkine
Senior Product Manager - Cell Culture
BioLife Solutions
Image Karen Langhauser
Editor-in-Chief
Cell & Gene Therapy Reviewt