Help with navigating the clinical research process
The following trainings and access requirements may be applicable to your study depending on the design or personnel needs. For each item, select the tile to see more information and determine which is right for you.
Applicable studies include any clinical research study conducted at Indiana University and/or IU Health that include a prospective component, provider services and/or require informed consent as defined by the Office of Clinical Research for Indiana.
In addition, pragmatic studies and studies requesting changes to the Electronic Medical Record (EMR) or clinical workflows are required to also follow the applicable requirements.
See more information about studies that should be registered in OnCore here.
Please see the tile legend below for steps that are required for ANY study vs. those that may be required if applicable.
Scroll down to see unique requirements for investigator-initiated research.
NOTE: The following steps may occur in parallel but generally flow from left to right.