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This article contains step-by-step instructions to complete and submit a Not Human Subjects Research (NHSR) protocol to the Office of Human Research Protections for review using the New WVU+kc IRB module.

There will soon be a new IRB Protocols module in WVU+kc! During the early-adoption phase, only NHSR type protocols should be submitted in the new module.

Information about accessing CITI training, what to do when trainings are not displaying in WVU+kc and where to ask questions regarding CITI training at WVU.

What to do if you receive the stack track error while trying to log into a CITI training module.

Details about the protocol submission process.

Frequently asked questions about submitting human subject research protocols to the IRB via WVU+kc.

Research Development acronyms for Kuali, eRA, Blue Sheet, Green Sheet, WVU+kc and IRB.

Follow these steps to submit your annual disclosure of conflicts of interest in research at WVU.

Track the routing and approval status of proposals and protocols submitted in WVU+kc.

How to convert an IRB form to .pdf to add a watermark.

How to make sure your CITI trainings display in WVU+kc.

Check if protocol is pending approval by PI, department chair or radiation/biosafety officers.

How to create and submit a registration for your clinical trial study in the WVU+kc application.
Registration with the Center of Excellence is required for all clinical trials on the Morgantown campus that meet the NIH clinical trial definition.

If a clinical trials registration is submitted by someone other than the Principal Investigator, it will come to the PI for approval. The principal investigator can edit the document to review or update content and then grant approval on the COE Actions page.

Fix for WVU+kc system undergoing maintenance error.