Social and health care registry data is a valuable resource for developing services, studying the well-being of the population, and finding new solutions for disease prevention and treatment. At the same time, it is essential to ensure that citizens’s health data remains protected and that no one’s privacy is compromised.
This course will help you understand what data is collected about us in social and health care, what the secondary use of social and health data means, why it is done, and how data is protected at every stage of the process.
Welcome to learn about the secondary use of health data!
Co-funded by the European Union. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or European Health and Digital Executive Agency. Neither the European Union nor the granting authority can be held responsible for them.
This training is provided as part of Findata’s advisory services. Please note that this course is not a comprehensive guide to the secondary use of health data, and Findata is not responsible for any subsequent changes to the information provided.
Curriculum
- 4 Sections
- 9 Lessons
- 30 Minutes
- Primary use of health data2
- Secondary use of health data2
- How is the privacy of health data ensured in secondary use?4
- Conclusion2
Instructor
