The UCR Registry Center has broad expertise and long experience. Here, more than 50 experts work on the design and organization of registers, economy, techniques, legislation, statistics, analyses, quality and scientific validation.

We utilize the latest technical solutions that enable us to offer totally innovative services such as development of medical devices in the form of software and registry-based randomized clinical trials.

The UCR Registry Center complies strictly with the legislation and regulations that govern the handling of national and regional quality registers. Just like our services and processes, how we process data is monitored by the Swedish Data Protection Authority.

You can find more detailed information on techniques, legislation and CE marking here.


Back to top