of Regulation (EU) 2018/1725 Sample Clauses

of Regulation (EU) 2018/1725. (37b) The secondary use of electronic health data can bring great societal benefits. The uptake of real-world data and real-world evidence, including patient-reported outcomes, for evidence-based regulatory and policy purposes as well as for research, health technology assessment and clinical objectives should be encouraged. Real-world data and real-world evidence have the potential to complement health data currently made available. To achieve this goal, it is important that data sets made available for secondary use by the present Regulation are as complete as possible. This Regulation provides the necessary safeguards to mitigate certain risks involved in the realisation of those benefits. The secondary use of electronic health data is based on pseudonymised or anonymised data, in order to preclude the identification of the data subjects.
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