Reset all


Content Types


AID systems



Data access

Data access restrictions

Database access

Database access restrictions

Database licenses

Data licenses

Data upload

Data upload restrictions

Enhanced publication

Institution responsibility type

Institution type


Metadata standards

PID systems

Provider types

Quality management

Repository languages



Repository types


  • * at the end of a keyword allows wildcard searches
  • " quotes can be used for searching phrases
  • + represents an AND search (default)
  • | represents an OR search
  • - represents a NOT operation
  • ( and ) implies priority
  • ~N after a word specifies the desired edit distance (fuzziness)
  • ~N after a phrase specifies the desired slop amount
Found 199 result(s)
The Research Data Center (RDC) “International Survey Programmes“ provides researchers with data, services, and consultation on a number of important international study series which are under intensive curation by GESIS. They all cover numerous countries and, quite often, substantial time spans. The RDC provides optimal data preparation and access to a wide scope of data and topics for comparative analysis.
The Finnish Social Science Data Archive (FSD) is a national resource centre for social science research and teaching. FSD archives, promotes and disseminates digital research data for research, teaching and learning purposes. Data descriptions are published in Finnish and English. Quantitative datasets are translated from Finnish to English on request. Several data are already in English. All services are free of charge. FSD promotes open access to research data, and transparency, accumulation and efficient reuse of scientific research. FSD is a national Service Provider for CESSDA ERIC.
The Data Catalogue (DBK) comprises the study descriptions from all studies archived at the Data Archive including study descriptions of historical studies data. The primary focus of the department “Data Archive for the Social Sciences” is providing excellent data service for national and international comparative surveys from the fields of social and political science research. These surveys, which must comply with clearly defined methodological and technical requirements, are archived and processed according to internationally recognized standards and made accessible to the scientifically interested public in a user-friendly manner.
DR-NTU (Data) is the institutional open access research data repository for Nanyang Technological University (NTU). NTU researchers are encouraged to use DR-NTU (Data) to deposit, publish and archive their final research data in order to make their research data discoverable, accessible and reusable.
The Integrated Fertility Survey Series (IFSS) is a project of the Population Studies aiming in view to produce a harmonized dataset of U.S. family and fertility surveys spanning five decades (1955-2002). IFSS integrates data from ten underlying component studies of family and fertility encompassing the Growth of American Families (GAF) in 1955 and 1960; National Fertility Surveys (NFS) in 1965 and 1970; as well as National Surveys of Family Growth (NSFG) in 1973, 1976, 1982, 1988, 1995, and 2002. The first release contains harmonized sociodemographic variables for all respondents from all ten component studies, including those related to marital status, race and ethnicity, etc. Thus it provides access to researchers, educators, students, policy makers, and others with a data resource to examine issues related to families and fertility in the United States. Potential users can download original/ harmonized datasets (along with documentation) and numerous analytic tools make it possible to quickly and easily explore the data and obtain information about changes in behaviors and attitudes across time.
The CDHA assists researchers to create, document, and distribute public use microdata on health and aging for secondary analysis. Major research themes include: midlife development and aging; economics of population aging; inequalities in health and aging; international comparative studies of health and aging; and the investigation of linkages between social-demographic and biomedical research in population aging. The CDHA is one of fourteen demography centers on aging sponsored by the National Institute on Aging.
The Twenty-07 Study was set up in 1986 in order to investigate the reasons for differences in health by socio-economic circumstances, gender, area of residence, age, ethnic group, and family type. 4510 people are being followed for 20 years. The initial wave of data collection took place in 1987/8, when respondents were aged 15, 35 and 55. The final wave of data collection took place in 2007/08 when respondents were aged 35, 55 and 75. In this way the Twenty-07 Study provides us with unique opportunities to investigate both the changes in people's lives over 20 years and how they affect their health, and the differences in people's experiences at the same ages 20 years apart, and how these have different effects on their health.
The Common Cold Project began in 2011 with the aim of creating, documenting, and archiving a database that combines final research data from 5 prospective viral-challenge studies that were conducted over the preceding 25 years: the British Cold Study (BCS); the three Pittsburgh Cold Studies (PCS1, PCS2, and PCS3); and the Pittsburgh Mind-Body Center Cold Study (PMBC). These unique studies assessed predictor (and hypothesized mediating) variables in healthy adults aged 18 to 55 years, experimentally exposed them to a virus that causes the common cold, and then monitored them for development of infection and signs and symptoms of illness.
The Johanna Mestorf Academy provides data from several archaeology related projects. JMA supports open access/open data and open formats. The JMA promotes research and education pertaining to the field of ‘Societal, Environmental, Cultural Change’ (Kiel SECC), which is one of the four research foci of CAU.
PSI is a global health organization dedicated to improving the health of people in the developing world by focusing on serious challenges like a lack of family planning, HIV and AIDS, barriers to maternal health, and the greatest threats to children under five, including malaria, diarrhea, pneumonia and malnutrition. A hallmark of PSI is a commitment to the principle that health services and products are most effective when they are accompanied by robust communications and distribution efforts that help ensure wide acceptance and proper use. PSI works in partnership with local governments, ministries of health and local organizations to create health solutions that are built to last. We use original data to monitor and evaluate our programs, generate consumer insight, estimate the impact of our solutions, and evaluate the health of the markets we work to strengthen.
The Australian Data Archive (ADA) provides a national service for the collection and preservation of digital research data and to make these data available for secondary analysis by academic researchers and other users. Data are stored in seven sub-archives: Social Science, Historical, Indigenous, Longitudinal, Qualitative, Crime & Justice and International. Along with Australian data, ADA International is also a repository for studies by Australian researchers conducted in other countries, particularly throughout the Asia-Pacific region. The ADA International data catalogue includes links to studies from countries including New Zealand, Bangladesh, Cambodia, China, Indonesia, and several other countries
The LISS panel (Longitudinal Internet Studies for the Social sciences) is the principal component of the MESS project. It consists of 5000 households, comprising 8000 individuals. The panel is based on a true probability sample of households drawn from the population register by Statistics Netherlands. Households that could not otherwise participate are provided with a computer and Internet connection. A special immigrant panel is available in addition to the LISS panel. This immigrant panel is comprised of around 1600 households (2400 individuals) of which 1100 households (1700 individuals) are of non-Dutch origin. Panel members complete online questionnaires every month of about 15 to 30 minutes in total. They are paid for each completed questionnaire. One member in the household provides the household data and updates this information at regular time intervals.
Goal of the psychology data archive PsychData is the documentation and long-term archiving of research data from all areas of psychology and the social sciences, using specially created metadata and to provide use of the data for scientific purposes such as secondary analysis and reanalysis. Psychdata contains all areas of psychology, in particular data sets from clinical, developmental, educational, gero-, and work and organizational psychology stemming from longitudinal studies, major surveys, and test development.
IDSC is IZA's organizational unit whose purpose is to serve the scientific and infrastructural computing needs of IZA and its affiliated communities. IDSC is dedicated to supporting all users of data from the novice researcher to the experienced data analyst. IDSC aims at becoming the place for economically minded technologists and technologically savvy economists looking for data support, data access support and data services about labor economics. IDSC is actively involved in organizing events (see our next Red Cube Seminar Talk) for data professionals, data analysts, and scientific data users and young researchers to discuss and share findings and to establish contacts for future cooperation.
The Global Terrorism Database (GTD) is an open-source database including information on terrorist events around the world from 1970 through 2015 (with annual updates planned for the future). Unlike many other event databases, the GTD includes systematic data on domestic as well as international terrorist incidents that have occurred during this time period and now includes more than 150,000 cases.
!!!the repository is no longer available, Please use: TheDataWeb at!!! This dataverse contains holdings from The DataWeb . TheDataWeb is the network of online data libraries and the infrastructure for intelligent browsing and accessing data across the Internet using the DataFerrett as the interface. TheDataWeb brings together under one umbrella demographic, economic, environmental, health, (and more) datasets that are usually separated by geography and/or organizations.
The Research Data Centre (FDZ-RV) was set-up in 2004 as an integral part of the German Federal Pension Insurance (Deutsche Rentenversicherung). Since then, the Research Data Centre produced several cross-sectional and longitudinal datasets, also called Scientific Use Files (SUF), available to researchers interested in issues of retirement, disability and rehabilitation. The datasets are released on an annual basis. The Scientific Use Files are subsamples drawn from the pool of individuals who are insured in the Federal Pension Insurance. The information provided in the original datasets is necessary to administer the beneficiaries of the pension insurance. is the Centers for Disease Control and Prevention primary online communication channel. provides users with credible, reliable health information on Data and Statistics, Diseases and Conditions, Emergencies and Disasters, Environmental Health, Healthy Living, Injury, Violence and Safety,Life Stages and Populations, Travelers' Health, Workplace Safety and Health
The Information Bank for Applied Research in Social Sciences (BIIACS) Central aims to provide strategic information services for the investigation and resolution of social problems and conduct rigorous analysis of databases and provide advice to decision-makers. To provide efficient access to information, the BIIACS conducted five major activities: collects, protects, preserves, and disseminates cure databases. The databases are available online and for free. They are organized in communities and collections with diverse content ranging from information on various economic, political and social of Mexico in different periods of federal government until election survey results conducted by higher education institutions as the CIDE and pollsters as Mund Americas.
The Comparative Agendas Project (CAP) assembles and codes information on the policy processes of governments from around the world. CAP enables scholars, students, policy-makers and the media to investigate trends in policy-making across time and between countries. It classifies policy activities into a single, universal and consistent coding scheme.
The Research Data Centre (FDZ) of the German Federal Employment Agency (BA) at the Institute for Employment Research (IAB) is intended mainly to facilitate access to BA and IAB micro data for non-commercial empirical research using standardised and transparent access rules. The FDZ mediates between data producers and external users. We also control for compliance with data protection regulations.
The National Digital Archive of Datasets (NDAD) provides access to archived datasets and documents from United Kingdom government departments which can be searched or browsed by subjects such as armed forces service or wills and death duties. Statistics and information gathered through census data as well as public records are used to compile the available datasets. All datasets are available to download and contain a record summary as well as custodial history, background on the source of the data and whether or not data may be added to the dataset in the future.