Understanding US-FDA Drug Submission Procedures September 9, 2007

The course is an in-depth analysis of the US-FDA regulatory requirements for INDs and NDAs. Practical tips will be given on the best way to communicate with the FDA: what they will expect from your applications and how to obtain the correctinformation from them.

Official Website: http://www.iir-events.com/IIR-conf/PTI/EventView.aspx?EventID=146