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Found 9 result(s)
The Human Mortality Database (HMD) was created to provide detailed mortality and population data to researchers, students, journalists, policy analysts, and others interested in the history of human longevity. The Human Mortality Database (HMD) contains original calculations of death rates and life tables for national populations (countries or areas), as well as the input data used in constructing those tables. The input data consist of death counts from vital statistics, plus census counts, birth counts, and population estimates from various sources.
Country
The Polar Data Catalogue is an online database of metadata and data that describes, indexes and provides access to diverse data sets generated by polar researchers. These records cover a wide range of disciplines from natural sciences and policy, to health, social sciences, and more.
Country
Supported by the DFG, the project „MO|RE data“ assembles a public eResearch-Infrastructure for motor research data until 2016. It focuses on selected standardized motor tests of wide acceptance. Furthermore MO|RE data generates quality authority control and publishes accompanying material for motor tests.
The Roper Center for Public Opinion Research is one of the world's leading archives of social science data, specializing in data from surveys of public opinion. The data held by the Roper Center range from the 1930s, when survey research was in its infancy, to the present. Most of the data are from the United States, but over 100 nations are represented.
Country
The WSI-Datenzentrum is a service provided by the Institute for Social and Economic Research (WSI). It collects and presents primary and secondary data on e.g. working conditions, co-determination or social policy. Primary data collected are primarily the WSI works councils surveys. Interested academics can use the works councils surveys collected from 2005 to 2011. The records are available to everyone and free of charge after contacting the repository owner and signing a data usage statement.
Contraceptive prevalence and the unmet need for family planning are key indicators for measuring improvements in access to reproductive health as asserted in the 2030 Agenda for Sustainable Development under target 3.7. "By 2030, ensure universal access to sexual and reproductive health-care services, including for family planning, information and education, and the integration of reproductive health into national strategies and programmes".