Anastassia is holding master’s degree in Biology and spent 5 years in cancer research laboratory to specialize thereafter in regulatory affairs, policy and patient engagement in the scope of clinical research. She was part of several IMI and EU funded projects, has been closely following the development and implementation of EU directives and regulations relevant to clinical research, including GDPR, but also others such as clinical trials regulation, in vitro medical device regulation, etc. After almost 20 years of work at headquarters of one of the largest European non-for-profit clinical research sponsor (EORTC), Anastassia joined MyData-Trust to bring her expertise at the service of a large circle of organizations active in life science.