eResearch Regulatory Management (eRRM) was updated on December 5, 2022. System changes in this release include the following updates:
Human Subjects Application (HUM)
The No CR Required and Exempt Annual Touch Point Message email notifications now include a link to initiate the study's Termination.
For IRB Staff
- The Reviewer Checklist item for Secondary Use studies involving stem cells now displays the FDA Regulated question.
- Updated auto contingency wording on the Reviewer Checklist.
- Updated the All IRBMED Amendments search report to include the application type of the parent application.
For COI Ancillary Committee members
The Ancillary Committee home workspace has a new lister on the Inbox for applications that COI staff have Advanced for IRB review.