Student Final Report Form - All students conducting research should submit this form to the Office of Research Compliance upon completion of their project.
Faculty Clinical Final Report Form- All faculty conducting clinical research should submit this form to the Office of Research Compliance upon completion of their project.
Faculty Final Report Form- All faculty conducting minimal risk research should submit this form to the Office of Research Compliance upon completion of their project.
FDA-1572-is a federal form and is the statement of the investigator that he/she will abide by the federal guidelines set forth in the Code of Federal Regulations for the use of drugs in an investigational setting.
Adverse Event Clinical-An adverse event is any occurrence or situation during the course of a research project that was: harmful to a subject taking part in the research, or increased the probability of harm to subjects taking part in the research. AE Clinical Form
Adverse Event Behavioral-The IRB definition of adverse event is an experience, the nature, severity, or frequency of which is not consistent with the current risk information described in the investigational plan, protocol, or consent form. AE Behavioral Form