In this webinar we will share with the audience VIVEbiotech´s approach for developing lentiviral vectors from very early stages to GMP, considering highly relevant aspects such as scalability, regulatory compliance, and cost-effectiveness. Different manufacturing steps such as transient transfection using the PEIpro® reagent from Polyplus-transfection will be described.
Attendees will grow their understanding of :
- LVV production requirements for scalability, regulatory compliance, and cost-effectiveness from early stages through to GMP.
- How an optimized production process can be adapted to several intermediate scales, streamlining various developmental phases.
- How to integrally manage LVV quality throughout the duration of the development project.
- Quality being a key feature of suitability for the final product, we will also overview concepts of quality control and quality assurance.