During the 2nd Workshop of EEFAM: Medical – 18 April 2019, the regulatory framework for clinical trials (interventional and non-interventional) was presented with special emphasis of the current legislation on their proper and legal management in relation to the European Personal Data Regulation (GDPR) and the European Regulation οf Clinical Trials (CTRs) was analyzed taking into consideration the purpose of processing clinical trial data, taking into account the active involvement of the patient in the research process and making the society as a whole socially relevant her upbringing.
