SYNTHIA aims to define the gold standard for building safe and effective synthetic data (SD) in the EU and beyond.

Our envisioned output and impact:

• Set the legal, ethical and regulatory framework for accelerating the adoption of SD for various healthcare applications, including regulatory decision-making
• Deliver a clinical-grade SD cohort for SYNTHIA clinical use cases and validate their application in clinical setting 
• Make research and results accessible to all healthcare stakeholders worldwide
• Leverage the use of SD for accelerating patients’ access to novel drugs, tools and devices, maximizing development of precision medicine while maintaining sustainability of EU healthcare systems

This page is under construction.