Cancer Registry of Norway, Institute of Population-Based Cancer Research
Norsk versjonAbbreviation
Kreftregisteret
Director
Frøydis Langmark
Address
Postboks 5313 Majorstuen, NO-0304 Oslo
Phone
(+47) 22 45 13 00
Fax
(+47) 22 45 13 70
kreftregisteret@kreftregisteret.no
Link
http://www.kreftregisteret.no/
Established
1951
Objective
The Cancer Registry’s primary goal is the establishment and dissemination of new knowledge which contributes to the reduction of cancer. The Cancer Registry Regulations, Regulations, by Royal Decree of 21st of December 2001 No. 1477, establish these main objectives of the Cancer Registry:
1. Registration: Collect and, within the scope of the Regulations, process data relating to cases of cancer and cancer studies in Norway in order to document the distribution of cancer in the country and describe changes over time,
2. Research: Conduct, promote and provide a basis for research to develop new knowledge of the causes, diagnosis, natural course and effects of treatment of cancer in order to improve and enhance the quality of preventive measures and medical assistance that are offered or provided to combat cancer, including the follow-up of individual patients and groups of patients,
3. Advice and counselling: Provide advice and counselling on medical assistance to combat cancer
4.Information: Provide information to other public administrative bodies and the population at large on measures that may prevent the development of cancer.
Present research
Epidemiological cancer research.
Ownership
Hospital Trust
Governing body
Board: 8 members
Turnover
110 mil. NOK (2008)
Sources of funds
Ministry of Health and Care Services, Norwegian Cancer Society, Confederation of Norwegian Business and Industry, Research Council of Norway, and others
Employees
150 (2009)
Number of R&D person-years
50-99
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Last updated on 12/05/2009 by Bo Sarpebakken