Writing Your HSIRB Protocol and the HSIRB Review Process

February 7, 2011

Julia Mays—Research Compliance Coordinator, WMU

To assist you with the HSIRB protocol and review process the Research Compliance Coordinator will discuss general HSIRB processes, levels of review, how to submit, and provide examples of research to help define “human subject research” under the Federal definition. Topics will include common errors that slow down the review process from submission to approval. If you are preparing to write a HSIRB protocol please consider attending as we will discuss applications, protocol outlines, and consent document requirements.

To access forms referenced in the presentation, please visit: http://www.wmich.edu/research/forms/complianceforms.html

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