Search Results for "Poverty Guidelines, Research"
Displaying 121 - 140 of 161 results. 20 results shown per page. Page 7 of 9.
January 7, 1999, Public Meeting of the Workgroup on National Health Information Infrastructure, NCVHS
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THIS TRANSCRIPT IS UNEDITED National Committee on Vital and Health Statistics
Procedings of the September 27-28 NCVHS Ad Hoc Meeting on the National Health Information Infrastructure
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National Committee on Vital and Health Statistics Ad Hoc Meeting on the National Health Information Infrastructure 12.30 p.m. September 27-28, 1999 Hubert H. Humphrey Building Washington, D.C.
Health Care Cost Containment and Medical Innovation
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ASPE ISSUE BRIEF Health Care Cost Containment and Medical Innovation May 2012 By: Amber Jessup, Ph.D.
Transcript of December 19, 2000 NCVHS Joint Hearings of the Workgroup on National Health Information Infrastructure and the Workgroup on Health Statistics for the 21st Century
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[This Transcript is Unedited]
Transcript of 2/3/99 Meeting of the Workgroup on National Health Information Infrastructure, NCVHS
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THIS TRANSCRIPT IS UNEDITED National Committee on Vital and Health Statistics
EHR Payment Incentives for Providers Ineligible for Payment Incentives and Other Funding Study
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Long-Term and Post-Acute Care Providers Engaged in Health Information Exchange: Final Report
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Personalized Health Care Expert Panel Meeting: Summary Report
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Contents Demonstrating Clinical Validity and Utility Demonstrating Value Reducing Health Disparities Educating and Engaging Providers and Consumers Using Databases to Build Eviden
Health Information Exchange in Post-Acute and Long-Term Care Case Study Findings: Final Report
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Rachael E. Bennett, MA, Mark Tuttle, FACMI, Karis May, Jennie Harvell, Med, and Eric A. Coleman, MD, MPH University of Colorado Health Sciences Center
Web-based Information Exchange and Information Services Concept to Support the Exchange of Newborn Screening Information
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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.
Web-based Information Exchange and Information Services Concept to Support the Exchange of Newborn Screening Information
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Web-based Information Exchange and Information Services Concept to Support the Exchange of Newborn Screening Information Office of the Assistant Secretary for Planning and Evaluation U.S. Department of Health and Human Services December 1, 2009
Improving Data for Decision Making: HHS Data Collection Strategies for a Transformed Health System: Implementation Update and Accomplishments
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Introduction and Background
Overview
The data collection systems sponsored by HHS are critical to the HHS mission, and they also provide most of the national statistical capacity to monitor the health of the population and the functioning of the health care, public health and human services systems.
Development of an Assistive Technology and Environmental Assessment Instrument for National Surveys: Final Report
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U.S. Department of Health and Human Services Development of an Assistive Technology and Environmental Assessment Instrument for National Surveys: Final Report Part I. Recommended Modules and Instrument Development Process
HHS Implementation Guidance on Data Collection Standards for Race, Ethnicity, Sex, Primary Language, and Disability Status
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October 2011
This guidance is available on the Internet at:http://aspe.hhs.gov/datacncl/standards/ACA/4302
Report to Congress on the Application of EHR Payment Incentives for Providers Not Receiving EHR Incentive Payments
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U.S. Department of Health and Human Services
Public Health-Related Activities for NHII
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NHII Home Coordinating Activities Public Health Related Activities
HHS Directory of Health and Human Services Data Resources - Introduction
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Overview The HHS Directory of Health and Human Services Data Resources is a compilation of information about virtually all major data collection systems sponsored by the U.S. Department of Health and Human Services (HHS).
Testimony by Joy Pritts for the January 27, 2003 NCVHS Workgroup onNational Health Information Infrastructure Hearings
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Georgetown University Institute for Health Care Research and Policy
Policy Statement on Inclusion of Race and Ethnicity in Dhhs Data Collection Activities
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SUMMARY: This document describes the Department of Health and Human Services (HHS) policy on the inclusion of racial and ethnic categories in HHS funded and sponsored data collection and reporting systems. This inclusion policy covers all programs of the Department, including both health and human/social services.
Case Studies of Electronic Health Records in Post-Acute and Long-Term Care
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U.S. Department of Health and Human Services