As cell and gene therapies progress through clinical trials and prepare for commercialization, it becomes increasingly critical for sponsors to pursue scalable solutions to overcome the imminent increase in risk. How can cell and gene therapy developers effectively prepare for a commercial environment that exists in an industry still in its infancy?
To increase potential for long-term success in both allogeneic and autologous programs, choosing partners with proven experience is essential. Leveraging service providers with specialized expertise, established global relationships and expansive infrastructure in place to collect, manufacture, deliver and provide required reporting for large quantities of therapies will ensure a smoother, faster transition to market, and ultimately, more patients.
Attendees will learn: