Armando Oliva is a physician-informaticist and entrepreneur with over two decades of leadership in biomedical and regulatory informatics, currently serving as President of Semantica LLC. He specializes in standardizing clinical trial data and electronic submissions to the FDA, having led data standards adoption and submission systems during senior roles at the FDA’s CDER and as Deputy Director for Bioinformatics. Armando blends clinical insight as a neurologist with technical expertise in biomedical ontologies and semantic web technologies (RDF/OWL) to drive semantic interoperability and automation for regulatory decision-making. He has founded and led consulting firms focused on translating policy and standards into practical submission and validation workflows. Based in Fort Lauderdale, he brings rare domain depth—MD training from Penn and a chemistry BA from Princeton—paired with hands-on experience shaping how clinical data are structured, validated, and used in regulatory review.
9 years of coding experience
13 years of employment as a software developer
M.D., Medicine, M.D., Medicine at University of Pennsylvania School of Medicine
B.A., Chemistry, B.A., Chemistry at Princeton University
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