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Join Kevin Smyth as he joins a live panel discussion and Q&A that will provide information and insight into recent and relevant regulations for ATMPs that can derail the approval process. From materials, cryopreservation, logistics, manufacturing, and facility design, this session will provide pragmatic strategies and tools to navigate the complex scientific and regulatory environment. Attendees will gain a greater understanding of ATMP cryopreservation, facility design, logistics, and regulatory classifications and will leave with the knowledge to assess complex subjects associated with ATMP production and have confidence in communication with regulators during interactions.

Get more information and register on the PDA Annual Meeting website.

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