Clinical Research

International Health Data from the Organization for Economic Cooperation and Development (OECD).

Data, statistics, and other tools and resources from the Centers for Disease Control and Prevention (CDC).

Research findings, data and statistical tools, reports and publications from Agency for Healthcare Research and Quality (AHRQ).

Division of the CDC that collects and reports accurate health statistics for better policy-making. Resource also provides information about publications, budget, and employment.

Tools and data from the Health and Human Services Operating Divisions for scientists, researchers, and the general public.

The All of Us database provides clinical, environmental, and social lifestyle data to inform how these factors affect health conditions, to promote the advancement of biomedical research such as precision medicine. The "Data Browser" public data is aggregated data from participants’ physical measurements, surveys, wearables, and electronic health records. In the "Researcher Workbench" Registered Tier, UNCW researchers can view and analyze within the Workbench platform individual (not aggregated) human subjects' de-identified biomedical data. Responsible Conduct of Research training within the platform is required for registration.

Health Data for states compiled by the Kaiser Family Foundation.

The Behavioral Risk Factor Surveillance System (BRFSS) is the nation’s premier system of health-related telephone surveys that collect state data about U.S. residents regarding their health-related risk behaviors, chronic health conditions, and use of preventive services. BRFSS completes more than 400,000 adult interviews each year, making it the largest continuously conducted health survey system in the world.

The vision for data dissemination through data.census.gov is to improve the customer experience by making data available from one centralized place so that data users spend less time searching for data content and more time using it.

The Census Bureau provides accurate, detailed, and up-to-date statistics—covering people and business—relating to health in America.

The CHR&R program provides data, evidence, guidance, and examples to build awareness of the multiple factors that influence health and support leaders in growing community power to improve health equity.

The Department of Population Health at NYU Langone Health and the Robert F. Wagner School of Public Service at NYU created the Dashboard as a health improvement planning resource for U.S. cities. The Dashboard continues to grow, and is a one-stop resource for viewing and comparing data from multiple sources on health and the factors that shape health to guide local solutions.

The Rural Health Information Hub, formerly the Rural Assistance Center, is funded by the Federal Office of Rural Health Policy to be a national clearinghouse on rural health issues.