Marina Romanova

Marina Romanova started their work experience in 2011 as a Clinical Trial Specialist at Teva Pharmaceuticals. Marina then joined Cromos Pharma in 2014 as a Regulatory Affairs Manager. After 4 years, they were promoted to Head of Regulatory Affairs and later became the Head of Moscow Office in 2019.

Marina Romanova attended First Moscow State Medical University named after I.M. Sechenov from 2007 to 2012, where they studied Pharmacy. Additionally, they have obtained various certifications, including "Introduction to Regulatory Affairs in the European Union" and "Introduction to Regulatory Affairs in the US and Canada" from the Regulatory Affairs Professionals Society (RAPS) in October 2022. Marina also holds certifications in GCP (Good Clinical Practice) and GVP (Good Vigilance Practices) from the Scientific Center for Expertise in Medical Application of the Ministry of Health of Russia. Furthermore, they have completed training in "General Principles of ICH GCP" from Matrix CRO and "Quality management in clinical research activities" from Susanne Zeller.