The Institutional Review Board is a local review board, established by the Western Michigan University Board of Trustees in accord with federal regulations, to interpret and apply federal regulations, ...

Potential research subjects must be accurately informed of what a project involves, and given the opportunity to decide of their own free will whether or not to participate. This process may be brief ...

Federal Regulations [45 CFR 46.103(b)(5) and 21 CFR 56.108(b)(1)] and UAB IRB policy (POL006) requires Principal Investigators of all human subject’s research (FDA-regulated or not), and their ...

Menu Collaborating With Researchers From Other Institutions Clinical Trials and Human Subjects Research Researchers must satisfy the requirements all of the institutions involved. It is the ...

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 ...

Unanticipated Problems that arise during human subjects research must be reported to the IRB as soon as possible - at the most within five business days of their being detected. See the “Submitting an ...

Purpose: Occasionally, external research personnel perform services that would not qualify them to count as officially part of the “research team.” However, situations are not always clear when those ...

The Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) has published data on involvement of the various subject areas in the 70 Clusters of Excellence funded under the federal and state ...

Investigators must use Cayuse to electronically submit new research studies for review and approval, course approvals, continuing research requests, amendments to approved research studies, and ...