Stephanie KromarSenior Regulatory Affairs Manager at EORTC
Stéphanie Kromar joined the EORTC in 2013. In 2014, she joined the Regulatory Affairs Department. As Senior Regulatory Affairs Manager, she is responsible for the preparation, submission and follow-up of Clinical Trials Applications from development until the end of trial. She has experience on VHP and recent pilot phases and provides regulatory advice. She is one of the Sponsor Product Owners under the new CTIS delivery model and has been involved in the implementation of the new clinical trials regulation from the firsts UATs till the recent on-site portal testing at EMA.