Live30 webinars are thirty-minute presentations designed to update you on the latest innovations, applications, and data in a fast yet interactive format.
The field of gene therapy manufacturing faces a significant hurdle in the form of a lack of process standardization. There are ways to address this challenge, however, such as using standardized methods, materials, analytics, and documentation. By implementing these measures, it is possible to minimize supply chain bottlenecks and increase manufacturing efficiencies and scalability. This, in turn, can lead to faster development timelines and smoother regulatory filings.
In this fireside chat, we will explore how a complete platform approach to fast-track AAVs can enhance quality and efficiency. This method can also help reduce manufacturing time while providing a well-suited process for late-stage clinical GMP production.
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