Post-IRB Approval Monitoring Calendar
The Post-IRB Approval Monitoring Program provides an annual calendar for researchers to help monitor special dates in regard to their research projects.
In addition to on-site monitoring of research, the post-IRB approval monitoring staff will also monitor the following issues:
- Reportable events in pre-submission for greater than two weeks;
- External monitoring reports received by the local study team for studies being conducted at ECU or its affiliates;
- ClinicalTrials.gov registration for studies where the primary investigator has indicated in ePIRATE that registration will be required; and
- Studies where a conflict of interest has been identified by the primary investigator in ePIRATE submission, ensuring a management plan has been provided and the appropriate language has been included in the informed consent document(s).
