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Human Subjects

Submission Requirements

In order to be ready to submit your study in KC IRB, you need to know the following information:

  • Principal Investigator name and department
  • Names of all other investigators (key and non-key)
  • Level of review of your study (see Level of Review for more assistance)
  • IND or IDE number (if applicable)
  • Where you’ll be conducting the research
  • The source of your funding, if you have funding
  • The number of subjects you would like to enroll in your study
  • Whether you will be enrolling any subjects who are a member of a vulnerable population.
    • Students
    • Children
    • Pregnant women/fetuses/neonates
    • Prisoners
    • Decisionally/cognitively-impaired individuals
    • Educationally/economically disadvantaged individuals
    • Transnational participants
  • Information on study procedures, recruitment strategies, risks/benefits, consent process, etc. as outlined in the KC IRB Crosswalk.
  • Protocol (required for Full Board studies)
  • Informed Consent Statement (if applicable)
  • HIPAA Authorization for Release of Health Information (if applicable)
  • Drug or Biological Products or Medical Device form(s) (if applicable)
If you plan on conducting research at the Roudebush VA Medical Center, more requirements apply. Please see the Forms & Templates page for more information.
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