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Gene therapy is rapidly advancing, yet rapid screening of optimal AAV viral vectors remains a key challenge. This is due to the time required for downstream purification and analytics, particularly the separation of the desired product from process- and product-related impurities.
This webinar introduces a novel high-throughput process and analytical development (HTPAD) platform designed to address these challenges by integrating Quality by Design (QbD) principles, automated purification, and at-line analytics. You will also learn about practical solutions that can help reduce time and cost while improving product consistency in AAV vector development.
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