This procedure outlines responsibilities of the investigator, OIRB and IRB for observation of the informed consent process in ongoing research.

This procedure outlines the responsibilities of the investigator, ORIB, and IRB to facilitate questions and concerns as part of the Informed Consent process.

This procedure lists responsibilities of the investigator, IRB, OIRB, and sponsor for waiver to the informed consent process in research planned for emergency settings.

This procedure outlines the responsibilities of the Investigator, OIRB and IRB regarding the informed consent process and documentation of informed consent.