Cell therapy has entered a new era. As autologous therapies continue to demonstrate durable outcomes and emerging modalities, including allogeneic, iPSC and in vivo approaches, expand into new therapeutic areas, sponsors face increasingly complex manufacturing decisions. A robust Chemistry, Manufacturing and Controls (CMC) strategy has become a critical driver of commercial success, influencing scalability, cost, product quality and long-term program viability. Join Catalent and BioPharma Dive for a discussion exploring how CMC strategies are evolving across cell therapy modalities and what sponsors can do today to prepare for tomorrow’s commercial landscape. Industry experts will examine manufacturing trade-offs, regulatory considerations, commercialization challenges and the strategic decisions that can help organizations build competitive, future-ready cell therapy programs. You’ll learn how to: Evaluate CMC strategies across different cell therapy modalities Balance manufacturing costs, scalability and commercial viability Understand evolving FDA guidance and its impact on development strategies Navigate centralized versus decentralized manufacturing approaches
