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Office of Science and Data Policy (SDP)

The Office of Science and Data Policy is the departmental focal point for policy research, analysis, evaluation, and coordination of department-wide public health science policy and data policy activities and issues. The Office provides authoritative advice and analytical support to the ASPE and departmental leadership on public health science policy and data policy issues and initiatives, coordinates science and data policy issues of interagency scope within HHS, and manages interagency initiatives in science policy and data policy. The Office works closely with staff from across the Department on strategic plan development and implementation efforts. The Offices also carries out a program of policy research, analysis, evaluation, and data development in these issues.

The Office of Science and Data Policy includes several components:

Topic Areas:

  • HHS Data Council
  • Regulatory Impact Analysis
  • Strategic Planning
  • Information Quality Guidelines
  • Prevention and wellness
  • Public health systems and functions
  • Food safety and nutrition
  • Drugs and devices
  • Tobacco control and prevention
  • Biomedical research and development
  • Economic analysis
  • Emergency preparedness, response, and recovery
  • Data and statistical policy
  • Health disparities and vulnerable populations
  • Health information technology
  • Microsimulation
  • Privacy policy

Reports

Displaying 111 - 120 of 156. 10 per page. Page 12.

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Web-based Information Exchange and Information Services Concept to Support the Exchange of Newborn Screening Information

State newborn screening (NBS) programs for heritable diseases and conditions provide vital health information that enables prevention and early detection of rare genetic conditions. Information management of the screening laboratory test orders and the reporting of laboratory is substantial challenge based on a variety of factors.

Identifying Opportunities to Maximize the Utility of Genomics Research Data Through Electronic Health Information Exchange

This report is a summary of the presentations and discussions at the workshop held by the Office of the Assistant Secretary for Planning and Evaluation, the National Cancer Institute, the Food and Drug Administration, and the Office of the National Coordination for Health Information Technology on October 15, 2009.

Electronic Reporting in Pathology: Requirements and Limitations

This white paper originated in the fall of 2008 from work carried out by the Pathology Electronic Reporting Taskforce (PERT) of the College of American Pathologists (CAP). Under contract support from the Centers for Disease Control (CDC), the PERT was tasked to propose electronic implementations of the CAP Cancer Committee's reporting templates.

Evaluation of the Personal Health Record Pilot for Medicare Fee-For Service Enrollees from South Carolina

Contract No: HHSP23320045020XI Prepared for: Ms. Suzie Burke-Bebee U.S. Department of Health and Human Services Office of the Secretary Assistant Secretary for Planning and Evaluation Prepared by:

Evaluation of the Personal Health Record Pilot for Medicare Fee-For-Service Enrollees from South Carolina

This mostly qualitative study identified key usability and utility components of a personal health record (PHR) being used by an elderly population living in South Carolina.

Economic Analysis of Availability of Follow-on Protein Products

Unlike most conventional drugs, biological products are usually large, complex molecules that are produced by living organisms. These commercially engineered biologics currently account for billions of dollars in health care spending.

Economic Analysis of Availability of Follow-on Protein Products

Contract HHSP23320045017XI Task Order HHSP233200700003T Prepared for: Department of Health and Human Services, Office of the Assistant Secretary for Planning and Evaluation Prepared by:

Consumer Use of Computerized Applications to Address Health and Health Care Needs

This paper examines consumer health needs that can be addressed through using health information technology, how consumers are using existing health information technology resources, differences in use by demographic group, what is necessary to expand its use, and related policy areas. [PDF - 49 pages]

Electronic Exchange of Clinical Laboratory Information Issues and Opportunities

The purpose of this paper is to conduct a study to enhance understanding of the current processes, issues and opportunities involved in the electronic exchange of laboratory information in ambulatory care settings, with a focus on safety-net clinics and federally qualified health centers.