Dr. Daniela Drago is Assistant Professor and Director of Regulatory Affairs Programs at The George Washington University’s School of Medicine and Health Sciences. Before joining academia, she held senior positions in the pharmaceutical and medical device industry. She worked in global regulatory and medical affairs roles at F. Hoffman-La Roche/Genentech, Vifor Pharma, Reckitt Benckiser, and Bausch & Lomb. Daniela contributed to more than 100 global regulatory submissions. Her current research interests focus on optimizing the development of FDA-regulated products and advancing regulatory science. Daniela received her Ph.D. in Chemistry from the Swiss Federal Institute of Technology (ETH Zurich).