Dr. Daniela Drago has served within the pharmaceutical industry, where she has held various positions in the regulatory arena over the last 10+ years. In her career Dr. Drago acquired extensive experience in global regulatory affairs, a broad knowledge of product regulations and significant expertise in managing and directing global regulatory teams. Dr. Drago has been working for companies ranging in size from start-ups to Fortune 100. She gained substantial know-how on strategic regulatory and operational activities for a wide range of product categories, ranging from prescription-only to over the counter (OTC) drugs, medical devices, cosmetics, nutritional and other regulated fast moving consumer goods. She has been leading and managing several pharmaceutical products to successful marketing approvals within US, Europe and other countries including emerging markets.