IRB Forms and Templates
Applications are designed to gather sufficient information for the IRB to determine that requirements for approval of research are satisfied. Please select from the drop-down menu and complete desired application. A description of each application, consent templates and other useful resources are also provided below the drop-down menu. Always refer to this page to ensure you are accessing the most current applications.
For any questions or concerns about IRB forms, please contact the IRB office at firstname.lastname@example.org or 609-258-0865.
Use this application to request review of newly proposed human subjects research that involves no more than minimal risk or greater than minimal research to participants.
Exempt Application (pdf)
Exempt Application (doc)
|Use this form to request exempt status for research with no more than minimal risk to subjects. This excludes research with prisoners, and some exclusions for children when research involves observation of public behavior where the investigator(s) participate in the activities being observed.|
|Not Human Research Determination||Use this form to request an official determination that a proposed project is not research, and does not involve involves human subjects.|
|Continuing Review Application||Use this form to request Continuing Review of approved non-exempt research. Continuing Review must be conducted prior to expiration of non-exempt research at least once per year.|
Modification Application (pdf)
Modification Application (doc)
|Use this form to request changes to approved research activities. Minor changes may be reviewed using expedited review procedures, but major changes must be reviewed at Full board meeting.|
|Report of Unanticipated Problems||Use this form to report Unanticipated Problems. Any unanticipated problems involving risks to subjects or others must promptly be reported to the IRB.|
Supplement A (pdf)
Supplement A (doc)
|Waiver of Consent|
|Supplement B||International Research|
|Supplement C||Research Involving Children|
|Supplement D||Cognitively Impaired Subjects|
|Supplement E||Stored Data for Future Use|
|Supplement F||Research Involving Drugs - Researching Involving Bioethics|
|Supplement G||Expedited Review Request|
|Standard Adult Consent||
Use this template to develop Informed Consent Forms and note that an informed consent is required for most prospective research with human subjects.
|INSTRUCTION AND GUIDANCE|
|Human Research Determination Guide||
This document provides an overview of IRB operations, describes when a project requires IRB review and lists common expedited and exempt categories of research typically conducted at Princeton
|Criteria for IRB Approval of Research||All criteria for approval of research must be satisfactorily met during IRB review before human subjects research may be approved by the IRB.|
|Protocol Requirements||This document provides a brief overview of essential factors which must be considered by the researcher prior to submission and during IRB review.|