Resource |
Audience |
Description |
Requirements |
Last Updated |
All Users |
Complete IRB10 training curriculum based on a user's roles in the system |
Required for all individuals who participate in the design, conduct, and/or reporting of FDA research |
8/29/2022 |
|
IRB Reviewers |
Guide for conducting reviews in IRB10 |
Not required |
8/29/2022 |
|
Study Staff |
Guide for all researchers on system activities and tools |
Not required |
10/14/2022 |
|
All Users |
Matrix with details on all ancillary committees and their review requirements |
Not required |
9/1/2022 |
|
All Users |
Quick guide to the required ancillary committee reviews and when to include as a reviewer |
Not required |
8/29/2022 |
|
All Users |
Details changes in fields from IRB8 (eProst) to IRB10 and what the mitigation plan is for each |
Not required |
8/29/2022 |
|
All Users |
Provides definitions for the study team member roles across all systems |
Not required |
8/29/2022 |
|
All Users |
Guide to understanding the functionality between the system integrations |
Not required |
10/14/2022 |
|
All Users |
Tip sheet on how to manage the guest list on submissions |
Not required |
9/13/2022 |
|
All Users |
Tip sheet on how to manage ancillary reviews on submissions |
Not required |
9/13/2022 |
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