The data collected in the cancer registries are used for various evaluations and publications.
The aims of the analyses according to the Cancer Registration Act are
- To monitor the development of cancer
- To develop and implement prevention and screening measures and check their effectiveness
- To evaluate the quality of care, diagnosis and treatment
- To support supply planning and research
The Federal Statistical Office, the National Agency for Cancer Registration (NACR) and the Childhood Cancer Registry use the data for analyses and publications.