A.37.3 Raw Data IOD Module Table


IE Module Reference Usage
Patient Patient C.7.1.1 M
Clinical Trial Subject C.7.1.3 U
Study General Study C.7.2.1 M
Patient Study C.7.2.2 U
Clinical Trial Study C.7.2.3 U
Series General Series C.7.3.1 M
Clinical Trial Series C.7.3.2 U
Frame of Reference Frame of Reference C.7.4.1 U
Synchronization C.7.4.2 C- Required if time synchronization was applied.
Equipment General Equipment C.7.5.1 M
Raw Data Acquisition Context C.7.6.14 M
Specimen C.7.6.22 U
Raw Data C.19.1 M
SOP Common C.12.1 M

Note: The Specimen Identification Module was previously included in this IOD but has been retired, and its functionality replaced by the Specimen Module. See PS 3.3-2008.