Orla Mc Callion has 20+ years of experience in the pharmaceutical industry. She is an accomplished scientist and leader within regulatory and clinical development. She regularly interacted with EMA, FDA and other national Regulatory Authorities for scientific advice procedures, submissions for serious conditions, orphan designations and pediatric-related activities and to secure clinical trial approvals. She was previously Director of Regulatory Affairs at OxThera AB. Orla holds a Ph.D. in Pharmacy from Queen’s University in Belfast.
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