The manufacture of rAAV continues to be challenged to incorporate faster, safer, scalable and cheaper critical starting material and manufacturing processes to meet timelines and regulatory demands.
TORONTO (PRWEB) March 16, 2023
The gene therapy clinical pipeline continues to be in a growth phase, with over 2,000 therapies in development globally, with recombinant adeno-associated viral vectors (rAAV) as one of the most powerful tools for gene delivery to treat human disease, leading the way.
The manufacture of rAAV continues to be challenged to incorporate faster, safer, scalable and cheaper critical starting material and manufacturing processes to meet timelines and regulatory demands. dbDNA™1 (Doggybone™), a novel enzymatic DNA technology, is a good critical starting material for rAAV production that can support the demands in the rapidly evolving gene therapy field and addresses the current challenges faced in rAAV manufacture.
In this webinar, the featured speakers will present the TAAV-manufactured enzymatic DNA process and product, featuring the advantages of the technology, such as regulatory benefits of using a bacterial-free DNA vector, leading to a more efficient and robust production. The speakers will discuss the quality control and assurance system that enables TAAV to provide a high quality product that can support an efficient rAAV manufacturing process throughout all phases of development from preclinical to clinical.
Join the featured experts to learn more about achieving a robust, scalable and high-quality DNA supply in recombinant adeno-associated viral vector gene therapy manufacturing.
1 dbDNA™ technology is licensed from Touchlight UK.
Join experts from TAAV Biomanufacturing Solutions, Dr. Leticia Agúndez, R&D Senior Manager; and Lucía San Miguel, Quality Senior Manager, for the live webinar on Tuesday, March 28, 2023, at 3pm EDT (12pm PDT).
For more information, or to register for this event, visit rAAV Manufacturing — Enzymatic DNA for Achieving a Robust & High-Quality DNA Supply.
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