IRB政策和程序
Step 1 – Does my Project Need IRB Approval?
All University of Idaho individuals whose activities meet both the definition of “human subjects” and of “research” are required to submit a Human Subjects Application Form to the Institutional Review Board and obtain approval or exempt certification prior to engaging in human subjects/participants research activities. If you are unsure whether IRB approval is required for your project, contact the IRB office at irb@kgfascist.com or 208-885-6340.
注意:
Have a question about the portal submission process?联系IRB协调员 irb@kgfascist.com or 208-885-6340
注意:
- Students are not eligible to serve as PI on IRB protocols. Their faculty sponsor can serve in this role to oversee the project.
- 审查APM 45.22 .保险单 PI资格要求.
注意:
We are implementing a three-year expiration date on all human subjects training beginning Jan. 1, 2016. After this date, protocols may be held for approval until the training has been updated.
Final approval is granted once the following have been completed:
注意:
Please confirm that your protocol has been approved before conducting any human subjects research. 欢迎联系 irb@kgfascist.com if you have any questions about the status of your protocol.
注意:
修订可包括, 但不限于, 程序/方法的变化, 人员, 参与者人群(年龄范围), 号), 招聘方法, 调查/面试问题 and consent/assent documents.
The PI or study contact is responsible for requesting an annual renewal of a protocol or closing the protocol when complete using the “Continuing Review and Closure Form” in 维拉. The 维拉 system will send reminder emails 60 and 30 days in advance of annual protocol expiration.
注意:
Noncompliance will be reported to applicable oversight agencies, 按照国土安全部的规定, OHRP, 食品及药物管理局和资金赞助协议.
注意:
Please close out all protocols once the project is complete. This can be completed by using the “Continuing Review and Closure Form” in 维拉.