Page History
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CRF Modules | Round # | Current Status of Module |
---|---|---|
2 | Final
| |
3 | Not Needed - Removed
| |
3 | Final
| |
4 | Under Review
| |
1 | Final
| |
4 | Under Review
| |
4 | Under Review
| |
3 | Not Needed - Removed
| |
4 | Under Review
|
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3 | Final
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2 | Final |
- Total of 5 CDEs built in one CRF standard module. |
3 | Internal Harmonization complete; Expanded Committee Review in session. | |
3 | Internal Harmonization complete; Expanded Committee Review in session. | |
4 | Internal Harmonization complete; Expanded Committee Review will follow Round 3. | |
3 | Internal Harmonization complete; Expanded Committee Review in session. | |
2 | Internal Harmonization complete; Expanded Committee Review completed. | |
4 | Internal Harmonization complete; Expanded Committee Review will follow Round 3. | |
4 | Internal Harmonization complete; Expanded Committee Review will follow Round 3. | |
3 | Internal Harmonization complete; Expanded Committee Review in session. | |
2 | Internal Harmonization complete; Expanded Committee Review completed. | |
2 | Internal Harmonization complete; Expanded Committee Review completed. | |
3 | Internal Harmonization complete; Expanded Committee Review in session. | |
2 | Internal Harmonization complete; Expanded Committee Review completed. | |
2 | Internal Harmonization complete; Expanded Committee Review completed. | |
4 | Internal Harmonization complete; Expanded Committee Review will follow Round 3. | |
3 | Internal Harmonization complete; Expanded Committee Review completed. | |
3 | Internal Harmonization complete; Expanded Committee Review in session. | |
4 | Internal Harmonization complete; Expanded Committee Review will follow Round 3. |
Introduction
The Standardized Case Report Form (CRF) Work Group is focused on establishing a core library of harmonized and standardized Phase II and III CRFs and data collection modules through stakeholder consensus. A core library of harmonized and standardized CRFs will be highly valuable to the cancer clinical trials community because it will provide a standardized mechanism for comparing and aggregating information across the NCI's clinical trial portfolio. Additionally, a harmonized CRF library will improve the efficiency and accuracy of the routine review of safety, efficacy, and administrative data from ongoing NCI-funded clinical trials. Finally, by reducing the time spent in developing a data collection strategy per trial, this core library will allow for faster initiation of new trials; thus, speeding the process of delivering new and improved treatments to patients.
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