When comprehensive registry data is more accessible to researchers and service providers, research and data-driven management become more efficient, resulting in:
- Better services for people, more effective medicines, health-promoting and supportive applications, and health technology.
- More efficient processes and service systems that better meet customer needs.
- More agile tools for monitoring and, for example, investigating adverse drug reactions.
Thus, citizens receive better and more impactful care and support, and disparities in health and well-being are reduced.
