Krabbameinsfélagið | Reykjavík is the brand behind the Icelandic Cancer Registry, a comprehensive database that registers all cancer cases in Iceland since 1955. The registry, established in 1954 by the Icelandic Cancer Society and the Directorate of Health, plays a crucial role in cancer epidemiology research in the country. It covers more than 99% of all cancer cases and operates under strict privacy and security policies.

The Icelandic Cancer Registry aims to prevent cancer, improve prognosis, and enhance the quality of life for cancer patients. It provides valuable information for quality control, genetic counseling, and scientific research. Researchers can access the registry with permission from the National Bioethics Committee.

In addition to the registry, Krabbameinsfélagið offers two other databases: The Cancer Detection Clinic Cohort Database, which collects information on reproductive and other risk factors from women attending cancer screenings, and The Family Database, which records family relationships. Both databases can also be accessed with permission from the National Bioethics Committee. With over 600 scientific research projects published in collaboration with national and international partners, the Icelandic Cancer Registry is a trusted source of epidemiological data.

The registry actively participates in international collaborations, such as the Association of Nordic Cancer Registries and the European Network of Cancer Registries. The Icelandic Cancer Registry is not only essential for cancer research but also provides valuable services to patients, including information for genetic counseling. With its focus on privacy, data accuracy, and collaboration, Krabbameinsfélagið | Reykjavík is at the forefront of cancer data management and research in Iceland