Figen Kabadas OgeSenior Regulatory Affairs Consultant at Informa
Figen Kabadas Oge holds over 15 years’ Regulatory Affairs experience in both small molecules and biologics at various stages of development with specific experience within EU, US and Turkey. She earned her B.S. in chemistry and two Master’s Degree in Regulatory Affairs and In-silico Drug Development in addition to an MBA in France. She has extensive experience in drug development, CMC, eSubmissions, drug development, IND, NDA, ANDA, CTA, MAA submissions, and life-cycle management. She is also a well-recognized RA trainer to the industry in Turkey and has been a speaker five times at Informa's GPRAS conferences since 2012.