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Tech Transfer and Manufacturing |

Tech Transfer and Manufacturing at Advanced Therapies Week 2026 Translating a promising therapeutic platform into a reproducible, GMP-compliant manufacturing process requires rigorous coordination across development and production teams. This panel brings together experts to discuss how biotech organizations can strengthen their technology transfer frameworks, improve scalability, and maintain product quality during rapid growth. Key takeaways 🔷 Define the core elements of a robust tech transfer framework for advanced therapies 🔷 Identify common challenges in scaling cell and gene therapy manufacturing 🔷 Evaluate approaches to maintain process comparability and product quality at scale 🔷 Discuss models for partnering with contract development and manufacturing organizations (CDMOs) 🔷 Explore digital and data-driven tools that enhance manufacturing readiness Chairperson James Cody (Associate Director - Technical Sales and Evaluations | Charles River Laboratories) Speakers Poh Yeh-Chuin (Head of Technical Ops | Tolerance Bio) Justin Skoble (Vice President of Technical Operations | Caribou Biosciences) Kumar Karyampudi (Senior Director & Site Head - Cell Therapy and Gene Engineering Facility | Moffitt Cancer Center) Nikki Bishop (VP - Marketing and Experience | Emerson) Gregg Nyberg (Chief Technology Officer | Landmark Bio)