IRBNet Forms & Documents
is a web based document management system. All GVSU research projects that require Human Research Review Committee (HRRC) approval must be submitted and stored on this system. Below are two sets of documents that you will need as you prepare to submit a research study for approval. These forms and instructions are also available in the IRBNet system in the FORMS LIBRARY on drop down menus. Any document may be downloaded and saved on a hard drive or removable storage device.
You must register on IRBNet and provide a valid e-mail address. Due to vulnerability and software interface needs, we recommend using a GVSU e-mail address rather than a commercial e-mail address. To register, go to: https://www.irbnet.org/release/public/register.jsp.
DO NOT USE THE DEMO VIDEO there. It is a marketing tool, not helpful for registering.
STUDENTS: If you are unsure of whether your planned research project requires HRRC approval, complete the Checklist for Student Protocol Submission (#1 in the Forms box below). Take your results to your research advisor who will help you determine if HRRC approval is necessary.
For new protocols, two actions are required. The first is completed by the researcher, the second is completed by the authorizing official. See the appropriate instructions in the Instructions for Submitting Materials box.
Submitting a NEW protocol study. Note: must include
- Application for New Protocol Review
- Supplemental Study Materials
- Signing (Authorizing/Approving) a study.
Additional forms also may be required depending on the nature of the research study. For questions, call (616-331-3197) or e-mail (email@example.com) the HRRC office.
After closing (completing) your study, you must complete the Closed Protocol Reporting Form. The protocol reporting form is a quick and easy way for the HRRC to collect required information from investigators about characteristics of their study. To complete the form, you will need the data from your study, including participant demographics.
Closed Protocol Reporting Form: http://www.gvsu.edu/hrrc/protocolreporting.htm
After submitting the Closed Protocol form online, please follow the instructions below (#7 - Closing a Research Study) to upload the form content to IRBNet.
|Instructions for Submitting Materials on IRBNet||
|0||Read This First||01/20/10|
|1||Submitting a New Protocol||01/20/10|
|2||Editing a Study Package after Submission||01/20/10|
|3||Signing a Research Protocol||01/20/10|
|4||Revising a Tabled Study||01/20/10|
|5||Change in Approved Protocol||01/20/10|
|7||Closing a Protocol||01/20/10|
|8||Unanticipated Problem/Serious Adverse Event||01/20/10|
|9||Guidance for Constructing an Informed Consent Document||03/10/10|
|1||Application for New Protocol Review||01/20/10|
|2||Change in Approved Protocol Form||01/20/10|
|3||Checklist Exempt Protocol||01/20/10|
|4||Checklist Expedited and Full Board Protocols||01/20/10|
|5||Checklist Student Research||01/20/10|
|6||Closed Protocol Reporting Form||01/20/10|
|7||Continuing Review Application Form||08/24/11|
|8||Exempt and Expedited Review Categories||01/20/10|
|9||GRPS Research Request Form||01/20/10|
|10||HIPAA Authorization Disclose PHI||01/20/10|
|11||HIPAA Authorization Future Recruitment||01/20/10|
|12||HIPAA Authorization Future Research Use||01/20/10|
|13||HIPAA Data Use Agreement||01/20/10|
|14||Individual Investigator Agreement Form (For non-GVSU students/staff)||01/20/10|
|15||Unanticipated Problem/Serious Adverse Event Reporting Form||01/20/10|
|16||GVSU Technology Statement. E-Survey Disclaimer||01/20/10|
Page last modified March 21, 2014