Natalya Eliseeva joined OCT in 2011. Natalya is responsible for the preparation and management of the regulatory applications and submissions. She ensures proper implementation of industry regulations and guidance documents. Together with the Clinical Department Natalya evaluates and reviews study materials for compliance with the current regulations and guidelines, oversees regulatory documents creation, dissemination and collection during study start-up, receives, reviews, files and maintains study-related essential documentation, reviews informed consent templates, obtains insurances, etc.
Natalya holds the Diploma of the Institute of International Trade and Law, Moscow. Natalya joined OCT as Office Manager and was then promoted to the position of a Regulatory Manager. Natalya's experience counts documents preparation and submissions to the Regulatory Authorities for more than 30 clinical trials.