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Evaluating the performance of Comparative Effectiveness Research Inventory against other databases.

Consolidating data and evaluating the utility of the Multi-Payer Claims Database.

Supporting expanded data infrastructure enhancements to the Chronic Conditions Data Warehouse to facilitate patient-centered outcomes research.

Establishing an infrastructure for the use of electronic health records in clinical comparative effectiveness research.

The Office of Human Services Policy (HSP) conducts policy research, analysis, evaluation, and coordination on various issues across the Department, including but not limited to, poverty and measurement, vulnerable populations, early childhood education and child welfare, family strengthening, economic support for families, and youth development.

The Assistant Secretary for Planning and Evaluation (ASPE) advises the Secretary of the Department of Health and Human Services on policy development in health, disability, human services, data, and science; and provides advice and analysis on economic policy.

Creating infrastructure for collecting data from patients through a mobile device application and enhancing data linkages.

Designing a web service for the public and researchers to be able to share interoperable technologies to address public health issues.

Linking and aggregating patient data to improve patient safety and privacy.

Convening working groups to determine common clinical outcome definitions and enhancing common definitions across data collection and reporting systems.

A working example to showcase the Food and Drug Administration’s guidance on electronic source data in clinical investigations.

Developing common data element standards for electronic health records.

Creating a Foundation to Advance the use of Artificial Intelligence for Patient Centered Outcomes Research and Clinical Practice

Providing PCOR Researchers with a Low Risk, Readily Available Synthetic Data Source

Validate and Expand Claims-Based Algorithms, Identifying Patients with Frailty and Functional Disabilities across Payer and Patient Populations

Strengthen the CRNs as a National Infrastructure for Technology Affecting Women’s Health

Establish a Surveillance Network across Multiple Clinical Sites to Rapidly Collect Data and Monitor Maternal, Infant, and Child Health Outcomes Related to Treatment for OUD During Pregnancy

Enhance Data Infrastructure and Increase Data Availability for Research on Parents with Substance Use Disorders

Leverage the Power of Administrative Data Resources and Accelerate Integration of Multiple Data Sources to Support Program Evaluation and Public Health Surveillance

Improve Public Health Surveillance and Expand Researchers’ Access to Data on Health Outcomes of Opioid Users with Co-occurring Substance and Mental Health Issues