Data registries collect, take care of, hold information. They make sure data is consistent and good quality. Surveys and epidemiological research reports use this data. Health services, such as hospitals and dialysis units, can add patient data to the Registry via forms and surveys. The registry records data on outcomes and treatment of kidney failure. The Australia and New Zealand Dialysis and Transplant Registry is the registry in Australia and New Zealand.
2. Data registries
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