Service mode | Document | Requirement | Note |
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data to go
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1. The application of data are clinical research database. 2. The application form clearly states the screening research populations. 3. In the screened research populations., the number of patients from each affiliated hospital is greater than five, and the number of medical records from each affiliated hospital is less than one percent of the total number of medical records in each hospital. |
To provide the screening criteria for research population, please complete the inquiry form APP01 (PICOTS). Certain datasets and columns have a higher re-identification risk due to free-text content. To protect patient privacy, only "report to go". For further details, please refer to the TMUCRD catalog. Selecting relevant columns will be regarded as use "report to go". A consultation form, APP01, must be submitted before the institute research review. When submitting, please fill“Data to go" in the “Suggestion or feedback”section, and include the application case number. Otherwise, the request will be processed as a general consultation case. |
report to go
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Based on statistical disclosure control, analysis results that are too detailed and less than one unit, or that can be deduced to less than one unit, or that are marked with special symbols shall not be permitted as report to go. Statistical analysis results that are permitted as report to go shall not be used to generate statistical results of less than one unit without approval. | To provide the screening criteria for research population, please complete the inquiry form APP01 (PICOTS). |
linked my data
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Based on statistical disclosure control, analysis results that are too detailed and less than one unit, or that can be deduced to less than one unit, or that are marked with special symbols shall not be permitted as "report to go". Statistical analysis results that are permitted as report to go shall not be used to generate statistical results of less than one unit without approval. | 1. During the review process, random checks will be conducted on the IRB informed consent. The informed consents will be returned immediately after inspection. 2. Linked files should be consistent with the file name, number of data items, columns name and code book on the IRB document. |
*TMUCRD releases update to 2021.12.31.
**Institutional research only provides two service modes: "report to go" and "linked my data".
***If you want to apply for specimens of TMU biobank and related clinical data, please contact JBB.
TMUCRD :