Sonia Sehra have overall 19 years of experience in core regulatory affairs. Her initial experience started with new submissions and post approval life cycle management including variations applications & renewals of WHO, South Africa, rest of Africa, South East Asia, China, Russia and CIS markets in Ranbaxy laboratories limited, Gurgaon, India ( now known as Sun Pharmaceuticals limited). She worked for different dosage forms like solid orals, solutions, suspensions, semi-solid dosage forms. Currently she is working with Mylan since last 9 years, and current profile includes post approval life cycle management of European markets, Australia, New Zealand, Japan and China markets. Responsible for life cycle management of more than 5000 MAs. Involved in facilitation of smooth launch of approved products. actively participated in various regulatory inspections.