Patients trust healthcare providers with their most sensitive data, but are their rights truly being upheld in practice? From the right to access medical records to the challenge of data portability and consent management, ensuring compliance becomes not only a legal requirement but also an ethical responsibility. This session tackles the real-world struggles of ensuring data subjects’ rights in the healthcare system and explores practical solutions for making compliance work for both patients and providers. 

Key questions 

• What barriers still exist in this context? 
• How can patient information be protected when they are shared internationally for research and telemedicine?
• What practical steps should be taken to ensure data subjects’ rights?