Spearheading Development of Gold Standard Donor Screening, Testing & Management to De-Risk Manufacturing, Improve Product Consistency & Performance & Meet Clinical Demand of High Quality Donor Material For Allogeneic Cell Therapies
Donor quality and strategy is the difference between promising allogeneic therapies and commercially viable products.
As more allogeneic programs progress into later-stage development, manufacturers are seeing first-hand how donor variability impacts yield, product consistency, cost of goods, and clinical performance. At the same time, regulators are demanding greater control and traceability of donor starting material, while investors increasingly expect evidence of scalable manufacturing. With competition from in vivo therapies intensifying, the industry can no longer afford to treat donor selection as a siloed upstream decision.
Fit-for-purpose donor strategies are emerging as a critical competitive advantage.
That's why the 4th Donor Selection & Cell Source Summit returns as the only dedicated forum focused exclusively on donor sourcing, screening, characterization, testing, and management for allogeneic cell therapies.
Join leaders from Bristol Myers Squibb, Senti Biosciences, Cellectis, Mesoblast, ImmuneBridge, Ernexa Therapeutics, and Indapta Therapeutics to explore how donor biology influences the entire therapy lifecycle. Through cross-functional discussions spanning process development, R&D, manufacturing, clinical development, and supply chain, you'll gain practical strategies to improve product performance, strengthen clinical outcomes, and improve manufacturing efficiency. Discover how the industry's leading innovators are transforming donor material from a source of variability into a driver of scalability, regulatory readiness, and commercial success.
Make your manufacturing processes and clinical outcomes reap the rewards of an optimized donor selection strategy.
Attending Companies Include