Controlled Interventional Clinical Study Sub-Task
(Redirected from Clinical Trial Subtask)
Jump to navigation
Jump to search
A Controlled Interventional Clinical Study Sub-Task is a inteventional clinical study sub-task within a clinical trial.
- Context:
- It can be referenced in a Clinical Trial Process.
- It can range from being a Phase I Clinical Trial Sub-Task (for a phase-1 CT), Phase II Clinical Trial Sub-Task, Phase III Clinical Trial Sub-Task, Phase IV Clinical Trial Sub-Task.
- It can include: Patient Recruitment (and be represented within a clinical trial process model).
- …
- Example(s):
- Clinical Trial Protocol Document Creation Task (to create a clinical trial protocol).
- Clinical Trial Site Selection & Initiation Task.
- Clinical Trial Participant Recruiment & Enrollment Task, composed of clinical trial recruitment, clinical trial screening, clinical trial consenting, ...
- Clinical Trial Study Execution Task.
- Clinical Trial Data Analysis Task.
- Clinical Trial Study Report Creation Task (to create a clinical study report).
- …
- Counter-Example(s):
- See: Clinical Trial Management System, Clinical Trial Phase.