FDA Compliance 2011 - Hands-On Workshop: Partnering for Drug Development in India

This unique conference is designed to provide hands-on training to non-Indian small and medium sized companies interested in exploring opportunities and understanding risks of conducting drug development in India for global product approvals.

This is a great opportunity for companies to explore the opportunities and hear from the experts who are involved or having deep understanding of the drug development in India.

This conference will Chaired by Dr. Mukesh Kumar PhD, RAC is the Head of Regulatory Affairs and Quality Assurance at Amarex Clinical Research and is on the Board of Amarex Biosciences India, He has been involved in about 100 clinical trials in more than 40 countries, has made several hundred regulatory submissions in US, India and EU.