Watch this webinar here: https://bit.ly/3jlcEXH Addressing the Challenge of Scalability in Viral Vectors To meet the ever-increasing demands for cell and gene therapies, there is a need to shift away from expensive, labor-intensive cell culture and scale up systems. But this goal cannot be met without a robust production strategy based on clinical indication, population size and dosing requirements. Early viral vector process development for cell and gene therapies is critical to assure a production strategy that supports commercial needs based on clinical indication, population size and dosing requirements. Most production processes today rely on labor-intensive and expensive adherent cell culture systems and scale out approaches. This webinar will highlight the importance of a scalable process that supports clinical through commercial needs. We will introduce a suspension-based process we have developed, including a HEK 293T cell line, chemically defined media, and optimized process conditions that results in higher yield, easier scalability, and lower production costs. In this webinar, you will learn: • Why suspension cell based processes are easier, faster, and more economical than adherent cell growth cultures • Use of chemically defined medium for improved cellular growth, viral productivity, easier downstream purification and improved safety from adventitious agents • Unraveling the complexities of the HEK293 and 293T cell lines • The importance of planning for scalability and manufacturability from the earliest stages of process development • How a scalable templated process can reduce time needed to move from product development to commercialization