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Cell & Gene Therapy Manufacturing & Commercialization Europe

Speaking Proposals Due 17th May

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Save the Date: 2-4 December 2024
Convention Centre DublinDublin, Ireland

Melody Dai
Executive Director, Regulatory Affairs at Adverum Biotechnologies
Speaker

Profile

Dr. Qing-Hong (Melody) Dai currently serves as Executive Director of Regulatory Affairs at Adverum Biotechnologies. She brings diverse experience in global regulatory affairs and drug development in the areas of ophthalmology, oncology, hematology and rare diseases. She spearheads the development and execution of CMC regulatory strategies for INDs, CTAs, and market applications throughout the clinical and commercial lifecycle management. Holding a Ph.D. in Biophysical Chemistry from Rutgers University and a B.S. in Chemistry from Peking University.

Agenda Sessions

  • Strategies for Ensuring Product Comparability in Gene Therapy Manufacturing: Case Studies and Regulatory Perspectives

    14:15