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Anna Koptina
Head of Regulatory Affairs,
Elicera Therapeutics
Anna is a seasoned Regulatory Affairs professional, specializes in cell and gene therapies within the field of immuno-oncology. Her expertise lies in strategic regulatory planning, navigating expedited programs, orphan designations, and fostering effective interactions with FDA, EMA and other regulatory authorities.
Sessions
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04-Sep-2025Theatre 1Panel: Engaging regulators early – The key to accelerating ATMP development