Clinical Research Track
Submitting WG/Project/Implementer Group
Clinical Interoperability Council
Clinical Research Studies currently require direct redundant entry of clinical data that should reside in EHR systems that conform to meaningful use. As data is managed in a pharmaceutical sponsor environment, the CRF data is updated, and may vary from the original source that presented by the EHR. This leads to difficulties for regulatory inspectors and reviewers in tracing back clinical data to source data, as well as redundant duplication of effort by site personnel, and general quality issues. Given the extreme cost and extended time required for randomized clinical trials, it would be substantially better to utilize EHR source data in clinical databases more efficiently.
Proposed Track Lead
Mitra Rocca, acting; other TBD
EHR vendors supporting FHIR API; Transcelerate BioPharma, Inc. EDC Vendors TBD
Please include information here regarding how much advance preparation will be required if creating a client and/or server.
This project will work with the Patient, DAF, and Structured Data Capture tracks to simulate data-related activities in pharmaceutical randomized clinical trials.
Role 1 Name
Form Designer - creates EDC form with variable mappings to FHIR API.
Form Manager – queries API to pull EHR data that maps directly to variables on eCRF.
Scenario Step 1 Name
- Success Criteria:
- Bonus point: