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Eugene Helsel

VP, Regulatory Affairs & Quality

Eugene Helsel brings more than 27 years of experience in the biotech industry with 20 years of experience in regulatory affairs and quality. His regulatory and quality experience has been focused on GMP compliance, chemistry, manufacturing, and controls (CMC), and preclinical studies specific to cellular and viral vector-based gene therapies. Pr...


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Roles at Artiva Biotherapeutics

  • VP, Regulatory Affairs & Quality

    Current role

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