Stephanie Tanimoto combines her experience in the medical device industry and healthcare field with excellent interpersonal and communication skills to effectively manage projects and help clients prepare for FDA meetings. Before coming to 3D, Stephanie held numerous positions in Clinical Research and Product Development at Allergan. While there, she helped develop clinical trial protocols, IRB submissions, created and delivered education training programs to physicians, and developed relationships with key opinion leaders and stakeholders across diverse scientific disciplines. Stephanie also was responsible for reviewing and analyzing scientific journals and literature to identify, analyze, and disseminate learnings. Stephanie has worked on clinical trials in the U.S., Europe, and Israel and is certified as a Clinical Research Professional. She has a strong foundation of knowledge and practice in research regulations, making scientific and clinical data relevant to both clinical and lay audiences.