| DICOM PS3.3 2019a - Information Object Definitions |
|---|
Table C.34.4-1 contains Attributes that identify a clinical trial context independent of any specific Clinical Trial Subjects.
Table C.34.4-1. Clinical Trial Context Module Attributes
|
The name of the clinical trial sponsor. See Section C.7.1.3.1.1. |
|||
|
Identifier for the noted protocol . See Section C.7.1.3.1.2. |
|||
|
The name of the clinical trial protocol .See Section C.7.1.3.1.3. |
|||
|
The identifier of the site responsible for submitting clinical trial data. See Section C.7.1.3.1.4. |
|||
|
Name of the site responsible for submitting clinical trial data. See Section C.7.1.3.1.5. |
|||
|
Name of the Ethics Committee or Institutional Review Board (IRB) responsible for approval of the Clinical Trial. Required if Clinical Trial Protocol Ethics Committee Approval Number (0012,0082) is present. |
|||
|
Approval number issued by committee described in Clinical Trial Protocol Ethics Committee Name (0012,0081). |
|||
|
The date the approval identified in Clinical Trial Protocol Ethics Committee Approval Number (0012,0082) becomes effective. |
|||
|
The date the approval identified in Clinical Trial Protocol Ethics Committee Approval Number (0012,0082) ceases to be effective. |
|||
|
The name of the institution that is responsible for coordinating the protocols for the clinical trial. See Section C.7.3.2.1.1. |
| DICOM PS3.3 2019a - Information Object Definitions |
|---|