Prior to completing an application, you will need to satisfy training requirements. The Human Subject Research Orientation on Canvas will ultimately save you time in ...

1. When composing your protocol, consider your readers. The IRB members are giving up their time to sit on the IRB and review research protocols – remember to respect their time and them. 2. Review ...

The Human Ethics module of ROAMWyo will streamline all aspects of human subjects research: protocol submission, review, and approval, as well as provide a dashboard where researchers can view the ...

Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include information about continuing reviews, amendments, event reporting (new ...

A protocol deviation or violation is any departure from the study procedures or treatment plans as specified in the IRB-approved protocol. Protocol deviations occur when an investigator does not ...

In order to address the specific details and regulatory requirements present in a retrospective medical chart review, the UB IRB recently created a new Protocol template: the HRP-503R. In order to ...