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Guidance in this section is applicable to TIG Nonclinical and Product Impact on Individual Health use cases only.In this section, the term "trial" is equivalent to "study" in the nonclinical context. The TIG guides implementation of the Trial Design datasets described in the following table below for use cases as indicated.
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| Metadataspec |
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| Num | Dataset | Description | Use Case(s) |
|---|
| 1 | Trial Arms (TA) | Represents each planned arm in the trial including the sequences of elements in each epoch for each arm. The TA and TE datasets are interrelated and provide the building blocks for subject-level information. | - Nonclinical
- Product Impact on Individual Health
| | 2 | Trial Elements (TE) | Represents the elements used in the trial including unique codes for each element, element descriptions, and the rules for starting and ending an element. The TA and TE datasets are interrelated and provide the building blocks for subject-level information. | - Nonclinical
- Product Impact on Individual Health
| | 3 | Trial Visits (TV) | Represents the planned order and number of visits in the trial within each arm. arm | - Product Impact on Individual Health
| | 4 | Trial Inclusion/Exclusion (TI) | Represents the inclusion and exclusion criteria for the trial.
| - Product Impact on Individual Health
| | 5 | Trial Summary (TS) | Represents key summary characteristics for the trial. | - Nonclinical
- Product Impact on Individual Health
| | 6 | Trial Sets (TX) | Represents planned sets of subjects that result from combinations of experimental factors defined for the trial. | |
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