Figen KABADAS OGE, Msc & MBA

Head of Regulatory Affairs at Delpharm

Figen Kabadas is Head of Regulatory Affairs with over 15 years' RA 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 Degrees in Regulatory Affairs and In-silico Drug Development in addition to an MBA in France.

She has extensive experience in drug development, IND, NDA, ANDA, CTA, MAA submissions, CMC, eSubmissions and life-cycle management.

She is also a well-recognised RA trainer to the industry in Turkey and she has been a speaker five times at Informa Connect Life Sciences Global Pharmaceutical Regulatory Affairs Summit since 2012.