• The Belmont Report
    The document that summarizes the basic ethical principles of research.

  • The electronic submission portal used to submit research submissions.

  • Comprehensive information regarding the federal regulations.

  • HHS agency that regulates clinical investigations products under its jurisdiction (drugs/biological products/medical devices).

  • Information from the Department of Health and Human Services on protecting human subjects in research.

  • Conditions under which protected health information may be used or disclosed by covered entities for research purposes.

  • A list of international agencies that oversee human subject research protections

  • An collection of informational resources pertaining to bioethics and biomedical research.

  • A graphic aid to help you decide if your research must be reviewed by the IRB.