A pharmaceutical industry professional who has worked in senior-level corporate positions, and as an independent consultant based in North America and India for clients in USA, Canada, Europe, India, China, Latin America, Africa etc., representing their interests in worldwide markets and health regulatory agencies.
Over 34 years of experience in global regulatory affairs, cGXP auditing, quality systems, compliance management, conceptualization, design and set-up of state-of-the-art manufacturing, testing and R&D facilities, strategic planning, business development, and international trade in the “regulated” as well as emerging (ROW) markets
Personal contacts in international markets, and extensive experience in interacting with health regulatory agencies in the USA, Canada, Europe, Australia, India, China, Latin America, Africa as well as the WHO (Geneva).