Establishing a robust and reproducible transfection process at large scale is a persistent challenge for teams manufacturing AAV and lentiviral vectors (LV). As batch volumes increase, differences in transfection complex preparation, incubation time, and transfer volume can introduce variability that impacts productivity, product quality, and development timelines. However, this has presented an opportunity for a novel solution.
This webinar examines how stabilizing transfection complex formation can support consistent performance as processes move from bench scale to clinical and commercial manufacturing. Attendees will learn how controlling continued transfection complex growth enables an expanded incubation window, supports more concentrated transfection complex preparations, and reduces the overall volume required for transfer into large production vessels. These improvements can simplify scale-up activities, reduce sensitivity to handling differences, and support more consistent productivity and product quality.
This session will also discuss practical considerations for implementing stabilized transfection workflows in large-scale manufacturing environments to streamline operations, minimize development risk, and reduce the need for repeated optimization as batch size increases.
Attend this webinar to:
You have registered for this webinar