Region · 10 records

Health databases & datasets: Nordic

Nordic health data — among the most complete population registries in the world, with personal identifiers enabling lifelong record linkage across health, prescription and social data.

Countries covered: Denmark, Finland, Norway, Sweden

SHOWING 10 OF 10 RECORDS

Danish National Patient Registry (Landspatientregisteret)

Danish Health Data Authority (Sundhedsdatastyrelsen) The Danish National Patient Registry contains comprehensive data on all hospital admissions, diagnoses coded in ICD-10, procedures coded in NOMESCO, and treatments in Denmark since 1977, covering both psychiatric and non-psychiatric inpatient care as well as emergency and outpatient specialty visits since 1995. Access for research is granted through application to the Danish Health Data Authority, which manages the registry as part of a broader health data system covering operations, diagnoses, births, causes of death, and medicines. Research database By application HDB-0113

Danish Civil Registration System (Det Centrale Personregister)

Ministry for Economic Affairs and the Interior (Denmark) The Danish CPR is a national register established in 1968 that maintains civil registration numbers, names, addresses, birth records, citizenship, church affiliation, parentage, and marital status for all Danish residents and Greenlandic citizens. Data is accessible to government agencies, businesses, organizations, and research institutions through data purchase arrangements, and individuals can request access to their own records. Research database Credentialed HDB-0114

Statistics Denmark

Statistics Denmark (Danmarks Statistik) Statistics Denmark is the central authority on Danish statistics that provides researchers and analysts access to a wide range of pseudonymised microdata about Danish society through its digital platform (DDP App). Authorised institutions can submit project proposals for approval to access microdata for research and analysis purposes. Research database Credentialed HDB-0115

Swedish National Patient Register (Nationella Patientregistret)

Socialstyrelsen (National Board of Health and Welfare, Sweden) The Swedish National Patient Register contains data on all inpatient hospital episodes since 1964 and outpatient specialist care visits, day surgery, and psychiatric care since 2001, including diagnoses, procedures, and administrative information. Access for research requires approval from the Swedish Ethical Review Authority following a formal application process. Research database By application HDB-0116

Swedish Prescribed Drug Register (Läkemedelsregistret)

Socialstyrelsen (National Board of Health and Welfare, Sweden) The Swedish Prescribed Drug Register contains records of all prescribed drugs dispensed in Swedish pharmacies since July 2005, with over 100 million entries annually, including patient age, sex, unique identifier, prescriber information, and dispensation details. The register is updated monthly and used by researchers, public agencies, journalists, and pharmaceutical industry representatives to study prescription patterns and drug safety. Research database By application HDB-0117

Norwegian Patient Registry (Norsk Pasientregister)

Norwegian Institute of Public Health (NIPH) The Norwegian Patient Registry contains information on all individuals who have received or are waiting to receive treatment in the specialist health service since 2008, including administrative, medical, and social information about healthcare episodes. Data access for research and other purposes requires submission of an application form to the Norwegian Institute of Public Health. Research database By application HDB-0118

Norwegian Prescribed Drug Registry (Legemiddelregisteret)

Norwegian Institute of Public Health (FHI) The Norwegian Prescribed Drug Registry is the successor to the Norwegian Prescription Database (NorPD) and contains records of all prescription drugs dispensed in Norwegian pharmacies since 2004, anonymised and pseudonymised for research use. Applications for research data access must be submitted to the Norwegian Institute of Public Health. Research database By application HDB-0119

FinnGen

FinnGen (public-private partnership) FinnGen is a large research project that has collected genome and longitudinal health data from over 500,000 Finnish biobank participants (approximately 10% of Finland's population), comprising more than 21.3 million genetic variants and over 2,750 health endpoints. Genome-wide association study (GWAS) results are publicly available for browsing and download, while complete dataset access is available to researchers at Finnish universities and university hospitals. Research database Free registration HDB-0120

Findata (Finnish Social and Health Data Permit Authority)

Findata (Finland) Findata is the Finnish authority that grants permits for the secondary use of health and social care data from multiple public and private data controllers, providing researchers access to pseudonymised registry data through a formal permit application process that typically requires 2-4 months for decision. The authority also pre-processes approved datasets and offers analytical tools for approved research uses. Research database By application HDB-0121

NORDCAN (Nordic Cancer Statistics Database)

Association of Nordic Cancer Registries (ANCR) and International Agency for Research on Cancer (IARC) NORDCAN is a web-based tool providing cancer statistics from Nordic countries (Denmark, Finland, Iceland, Norway, Sweden, Faroe Islands, and Greenland) including incidence, mortality, survival, and prevalence data spanning up to 70 years, with the earliest records from Denmark's National Cancer Registry established in 1943. Data is updated annually and presented as anonymous, privacy-protected statistics that can be compared across countries, regions, cancer types, and demographic groups. Research database Open access

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