Global Health Data Exchange - Discover the World's Health Data

Series and Systems

Survey families or dataset series are data collection efforts that occurred over a period of time or in several geographic locations, using the same or very similar data collection methodology and instruments. Series may be multinational -- collected in more than one country -- or in a single country. Usually all the datasets in the series are collected with the support of the same institution or institutions, but individual surveys or datasets may have the support or assistance of additional parties. The advantage of series from a research perspective is that often data from a series are more easily comparable than data from a variety of sources.

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The INDEPTH Study on Global Ageing and Adult Health provides data on ageing populations living within the INDEPTH health and demographic surveillance sites (HDSS).
Saint Kitts and Nevis Reported Deaths includes monthly deaths by sex, first-level administrative division (island), and year. This table does not include age detail.
The Samoa Demographic and Health Survey (SDHS) provides estimates of Samoa’s demographic and health situation.
The registry collects data on all new cases of cancer including primary malignant neoplasms, carcinoma in situ, neoplasms of uncertain behavior and benign brain and spinal cord tumors.
Singapore Birth Defects Registry includes tabulations of birth defects among resident population live births by gestation period from the Singapore Birth Defects Registry.
The Singapore Cancer Registry is a comprehensive population-based cancer registry that began in January 1968. In April 2001, it came under the auspices of the National Disease Registries Office (NDRO).
Survey series conducted for surveillance of the HIV epidemic in South Africa.
South Africa Recorded Live Births includes annual vital registration live births data. This release includes a report and microdata.
This system collects data on live births, stillbirths, deaths and marriages.
The Central Cancer Registry was established in 1980. It collects, manages, analyzes, and distributes data including cancer incidence and survival, including annual reports and other statistics.

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