Introduction This session will review the interplay among European regulations for health and medical data. The panel will discuss how the regulatory framework shapes the future of medical research and innovation, with a special focus on the interplay between the AI Act, Medical Device Regulation (MDR), and the European Health Data Space (EHDS), and their collective impact on medical ...

Join professionals and experts from esteemed institutions united in the commitment to upholding the highest standards of data integrity and privacy in the medical field. This Track sets the stage for enlightening discussions, insightful presentations, and collaborative exchanges aimed at fostering compliance excellence in healthcare data management.  

Introduction This session will focus on the adoption of the European Health Data Space (EHDS) regulation and its implications in terms of obligations and compliance. It will share the views of the European Commission and experts in this field. The speakers will also discuss the practical implementation of EHDS, in addition to the challenges and opportunities it presents.  

Introduction This session will focus on the secondary use of data in the health and medical sector, with a special focus on the needs and challenges of practitioners, including in the medical research domain. From healthcare to research and beyond, the speakers on this panel will offer an insight into the evolving needs, barriers, considerations, frameworks, and challenges associated ...

Introduction This session will present and discuss innovative technologies and methodologies aimed at overcoming the barriers associated with secondary data use. Speakers will focus on solutions and innovative approaches for data reuse, including synthetic data generation, federated machine learning, and self-assessment methodologies. They will also unveil how these approaches are sha...

Introduction This session will discuss and compare the value of synthetic data, pseudonymized data, and anonymized data for medical research. Beyond the ethical dimension and their relevance for data protection by design, the session will discuss their relevance for medical research.  Key questions and objectives ...

Introduction In the field of healthcare data processing, consent has long been considered the primary legal basis. However, with evolving medical research and innovation, alternative legal bases are gaining more attention. This session will discuss and review these alternative approaches to support lawful medical data processing.  

Introduction Medical research often requires accessing large data sets from various geographic regions to avoid any bias in the results. This session will discuss the needs, opportunities, and challenges for sharing medical data beyond borders. The EHDS provides a mechanism for such international cooperation. How will it work in practice? What are the constraints in other jurisdiction...