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WP 4. National standard for registry data documentation

The main objective of WP 4 is to establish the HRR metadatabase, which is an online collection of variables from the central health registries. The metadatabase contains no sensitive information, but provides information about research data to which researchers may have access. Such information is useful for researchers who would like to outline a research project and for applications for ethical approval and access to data. The metadatabase will also useful for executive officers in ethics committees and registers who consider these applications.


Contact information
Inger NjĂžlstad (leader of WP 4)
Hans-Henry Jacobsen (WP 4)
Inge Voldseth (WP 4)