I have a Masters degree in Pharmacy and have been working in the industry for 12 years, primarily in the field of international drug regulatory affairs. I am regulatory expert familiar with EU/ROW standards, dealing with e-filings, the generation of CTD/ACTD registration dossiers and Investigational Medicinal Product Dossiers (IMPDs). I also have experience in the field of medical supplies, hospital equipment and furniture. My intimate knowledge of the business, including its finer nuances gives me an edge in a crowded field where product differentiation is often hard to perceive.I am an avid reader and love to travel.