The Risk Assessment Document enables access to clinical data and provides a framework for secure consultation. This document complies with the following regulatory references: European Regulation 2016/679 (GDPR), Legislative Decree 101/2018, Clarifications on the application of regulations for processing health data in the healthcare sector – March 7, 2019, Ethical guidelines for processing for statistical or scientific research purposes published pursuant to Article 20, paragraph 4, of Legislative Decree No. 101 of August 10, 2018 – December 19, 2018, Legislative Decree No. 196/2003, the so-called Privacy Code, and Decree-Law No. 19 of March 2, 2024, coordinated with the Conversion Law No. 56 of April 29, 2024. This agreement stands as a significant milestone in the UIMOLS project. Its significance lies not only in its immediate support of our current objectives but also in its role as a foundational framework for future endeavors. Moreover, this agreement establishes strong rules and standards, laying the groundwork for future collaborations that might use similar arrangements for beneficial outcomes.
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