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Approximately 60 000 malignant cases of cancer is registered every year in Sweden. It is compulsory for every health care provider to report newly detected cancer cases to the registry. Population registration in Sweden (Swedish: folkbokföring) is the civil registration of vital events (e.g. births, deaths, and marriages) of the inhabitants of Sweden. The data is kept in the population registry (folkbokföringsregister) and is administered by the Swedish Tax Agency (Skatteverket).

Sweden registry data

The data is kept in the population registry (folkbokföringsregister) and is administered by the Swedish Tax Agency (Skatteverket). All five Nordic countries (Denmark, Finland, Iceland, Norway and Sweden) have nationwide registries containing virtually all individuals residing in those countries. The similarities between the registries in the Nordic countries make it possible to combine the registry data of each separate country into one larger cohort. The National Breast Cancer Register (NBCR) of Sweden was launched in 2008 and is used for quality assurance, benchmarking, and research.

This option is for when you want information on Swedish businesses only, as a one-off purchase. Search for the business or person in the field below.

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Data on the patient. Personal identification number; Sex; Age; Place of residence; 2.

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Part 2 of the registration certificate is a valuable document and must always be sent in with an application for a change of ownership, even in cases where the change of ownership is made to a car dealer. Sweden Switchboard: +46 8 405 10 00.

Sweden has a system of unique personal identity numbers that allows researchers to link data from different registers to … Validity of information on gynecological operations in the Swedish in-patient registry. Other. The Swedish Hip Fracture Register and National Patient Register were valuable for research on hip fractures: comparison of two registers. Bullous Pemphigoid: Validation of the National Patient Register in Two Counties in Sweden, 2001 to 2012 Statistics Sweden’s Business Register is a register of companies and local units in Sweden.
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The regionalization implies a close contact between the registry and the reporting physician, which in turn simplifies the task of correcting and checking the material.

Registers of interest from a research point of view can be divided into national public authority registers, quality records in healthcare, biobanks and research-generated data.
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Select product (s) Pay by card. Receive an email with a link to the product (s) The product is available for download for 48 hours. The e-service falls under the Terms for access By signing up to a digital mailbox service or by registering your email address with Bolagsverket, you can minimise the risk of your company being hijacked. The Swedish Twin Registry The Swedish Twin Registry, managed by Karolinska Institutet is the largest of its kind and has become an invaluable resource for medical research.

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The Swedish Hip Fracture Register and National Patient Register were valuable for research on hip fractures: comparison of two registers. Bullous Pemphigoid: Validation of the National Patient Register in Two Counties in Sweden, 2001 to 2012 Statistics Sweden’s Business Register is a register of companies and local units in Sweden. It contains all legal persons. Pursuant to a decision by the Swedish Riksdag, Statistics Sweden has been tasked, since 1963, to maintain a central business register. Official Registry Data On the following pages, you can find information collected from the Swedish official registries for the ULSAM cohort. The regionalization implies a close contact between the registry and the reporting physician, which in turn simplifies the task of correcting and checking the material. Information available in the Swedish Cancer Register.

Patient-Reported Outcome Measures and Risk Factors in a

Official Registry Data On the following pages, you can find information collected from the Swedish official registries for the ULSAM cohort. The regionalization implies a close contact between the registry and the reporting physician, which in turn simplifies the task of correcting and checking the material. Information available in the Swedish Cancer Register. There are three different types of information: 1. Data on the patient. Personal identification number; Sex; Age; Place of residence; 2.

It was driven, as many of their registries are, by a professional organization, the Swedish Orthopedic Society. Its success inspired the growth of other similar initiatives, and their use to help lower costs and improve outcomes.