Enhancing Data Resources for Researching Patterns of Mortality in Patient-Centered Outcomes Research |
Centers for Disease Control and Prevention
Food and Drug Administration
Centers for Medicare and Medicaid Services
|
FY 2017 |
A Synthetic Health Data Generation Engine to Accelerate Patient-Centered Outcomes Research |
Office of the National Coordinator for Health Information Technology |
FY 2019 |
Identifying Co-Occurring Disorders among Opioid Users Using Linked Hospital Care and Mortality Data: Capstone to an Existing FY18 OS-PCORTF Project |
Centers for Disease Control and Prevention |
FY 2019 |
Assessing and Predicting Medical Needs in a Disaster |
Office of the Assistant Secretary for Preparedness and Response
Agency for Healthcare Research and Quality
|
FY 2018 |
Emergency Medicine Opioid Data Infrastructure - Key Venue to Address Opioid Morbidity and Mortality |
National Institutes of Health |
FY 2018 |
Capstone for the Outcomes Measures Harmonization Project |
Agency for Healthcare Research and Quality |
FY 2018 |
Strengthening the Data Infrastructure for Outcomes Research on Mortality Associated with Opioid Poisonings |
Centers for Disease Control and Prevention |
FY 2018 |
Childhood Obesity Data Initiative (CODI): Integrated Data for Patient-Centered Outcomes Research Project |
Centers for Disease Control and Prevention |
FY 2018 |
Technologies for Donating Medicare Beneficiary Claims Data to Research Studies |
Centers for Medicare and Medicaid Services (CMS)
National Institutes of Health
|
FY 2017 |
Developing a Strategically Coordinated Registry Network (CRN) for Women’s Health Technology |
Food and Drug Administration
National Institutes of Health
Office of the National
Coordinator for Health Information Technology
|
FY 2017 |
Harmonization of Various Common Data Models and Open Standards for Evidence Generation |
Food and Drug Administration
National Institutes of Health
Office of the National Coordinator for Health Information Technology
|
FY 2017 |
Advancing the Collection and Use of Patient-Reported Outcomes (PROs) through Health Information Technology (IT) |
Agency for Healthcare Research and Quality
Office of the National Coordinator for Health Information Technology
|
FY 2017 |
PCOR: Privacy and Security Blueprint, Legal Analysis and Ethics Framework for Data Use, & Use of Technology for Privacy |
Centers for Disease Control and Prevention
Office of the National Coordinator for Health Information Technology |
FY 2015 |
Use of the ADAPTABLE Trial to Strengthen Methods to Collect and Integrate Patient-reported Information with Other Data Sets and Assess Its Validity |
National Institutes of Health |
FY 2016 |
Standardization and Querying of Data Quality Metrics and Characteristics for Electronic Health Data |
Food and Drug Administration |
FY 2016 |
Utilizing Data from Various Data Partners in a Distributed Manner |
Food and Drug Administration |
FY 2015 |
Improving the Mortality Data Infrastructure for Patient-Centered Outcomes (PCOR) |
Centers for Disease Control and Prevention |
FY 2015 |
Development of a Natural Language Processing (NLP) Web Service for Public Health Use |
Centers for Disease Control and Prevention
Food and Drug Administration
|
FY 2016 |
Security and Privacy Standards for Patient Matching, Linking and Aggregation |
Office of the National Coordinator for Health Information Technology |
FY 2015 |
Harmonization of Clinical Data Element Definitions for Outcome Measures in Registries |
Agency for Healthcare Research and Quality |
FY 2016 |
Source Data Capture from Electronic Health Records: Using Standardized Clinical Research Data |
Food and Drug Administration |
FY 2016 |
Creation of LOINC Equivalence Classes |
National Institutes of Health |
FY 2016 |
Cross Network Directory Service |
Food and Drug Administration |
FY 2015 |
Collection of Patient-Provided Information through a Mobile Device Application for Use in Comparative Effectiveness and Drug Safety Research |
Food and Drug Administration |
FY 2015 |
Conceptualizing a Data Infrastructure for the Capture and Use of Patient-Generated Health Data |
Office of the National Coordinator for Health Information Technology |
FY 2015 |
Improving Beneficiary Access to their Health Information through an Enhanced Blue Button Service |
Centers for Medicare and Medicaid Services |
FY 2016 |
Improving Beneficiary Access to Health Information: A Plan to Enhance “Blue Button” |
Centers for Medicare and Medicaid Services |
FY 2014 |
Strengthening and Expanding the Community Health Applied Research Network (CHARN) Registry to Conduct |
Patient-Centered Outcomes Research (PCOR)
Health Resources & Services Administration
|
FY 2014 |
Creating the Foundational Building Blocks for the Learning Health Care System: Data Access Standards for Electronic Health Records (EHRs) |
Office of the National Coordinator for Health Information Technology |
FY 2013 |
Creating the Foundational Blocks for the Learning Health Care System: Structured Data Capture (SDC) |
Office of the National Coordinator for Health Information Technology |
FY 2013 |
Expanding Data Collection for the National Program of Cancer Registries (NPCR) for Comparative Effectiveness Research (CER) |
Centers for Disease Control and Prevention |
FY 2013 |
Comparative Effectiveness Research (CER) Inventory |
Assistant Secretary for Planning and Evaluation |
FY 2012 |
Beta Testing the Multi-Payer Claims Database (MPCD) |
Assistant Secretary for Planning and Evaluation |
FY 2012 |
Maintenance and Support of the Chronic Conditions Warehouse (CCW) for Comparative Effectiveness Research (CER) |
Centers for Medicare and Medicaid Services |
FY 2012 |
Development of Data Infrastructure for Use of Electronic Health Records (EHRs) in Comparative Effectiveness Research (CER) |
Office of the National Coordinator for Health Information Technology
National Institutes of Health
|
FY 2012 |