Welcome to our guide to the IRB process at Saint Louis University. If you’ve made it through the considerations on our Getting Started page and determined that you need IRB approval for your research, this section will take you through next steps.
In general, the IRB process includes:
- Creating and submitting your IRB application for IRB review
- Receiving a request to make any necessary revisions to obtain IRB approval
- Getting notice of your IRB approval – now you can begin your research project
- Conducting the research exactly as approved by the IRB
- Submitting necessary forms during the conduct of the study, such as: an amendment to change the protocol, a continuing review to extend the expiration, other reportable events and a final report to close your study.
This section has the forms, guidance and information you need for the various phases of the IRB process. Select from the options below.
This page will help you design your study and develop an IRB Application. The “Sample Protocols” link will take you to a portal of already approved SLU IRB Applications organized by type of research. For clinical researchers, we’ve provided links to helpful NIH protocol design tools and templates.
This page will help you prepare and submit an IRB Application. It will guide you to the right forms, provide helpful tools for our eIRB system, and list upcoming meeting dates and submission deadlines for higher risk studies that require full board review by the convened IRB Committee. You can also learn about Scientific Pre-Review requirements for unfunded studies and more.
This page will help you prepare and submit an IRB Application to an approved external/central IRB. Using an external or central IRB for IRB review still requires an abbreviated submission to the SLU IRB Office for local administrative review and pre-authorization. This page includes forms and helpful tools to guide you through this process. It also contains information on IRB expectations for conducting IRB-approved research and the forms and guidance you may need along the way.
The IRB expects you to conduct your study exactly as it was approved unless an amendment is submitted and approved by the IRB prior to implementing changes. This section contains information on IRB expectations for conducting IRB-approved research and the forms and guidance you may need along the way.