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IRB Meeting Dates and DeadlinesIs It Human Subject Research?Templates and Samples
  • Training and Education

    The University of Mississippi Medical Center requires all individuals directly involved in the conduct of human subjects research to complete human subjects protection training before study involvement may begin.  IRB approval will be withheld until the training requirement has been met by the Principal Investigator.  

    To whom does this policy apply?

    This requirement applies to all persons who have a significant role in the research.   All of these individuals should be listed as study personnel in the IRB application.

    Examples include:

    • Principal Investigators and Co-investigators
    • Individuals named on a study grant or contract proposal
    • Individuals listed on an FDA form 1572
    • Individuals named as a contact person in the informed consent document(s) or recruitment materials for research
    • Individuals who obtain informed consent from research participants
    • Individuals who obtain individually identifiable information


    What training is required?

    The CITI initial Human Subjects Research course (either biomedical or social-behavioral) 

    How often is training required?

    Every 3 years

    You will be required to take the applicable refresher courses every 3 years

    Verify CITI training status:

    To obtain proof of your IRB education or dates of training, you may log into the IRB database, IDEATE, and view or print your education profile screen. That screen will list each program you have taken and the applicable dates.

    Password Assistance:

    To obtain assistance with requesting your password please call CITI at 305-243-7970.


    CITI website: