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Clinical Studies Center Services
The Clinical Studies Center (CSC) offers a variety of services that help investigators ensure compliance with human studies regulations and good clinical research practices.

These services include training and education for research staff, assistance with Emory IRB and R&D Committee protocol submissions, informed consent review and reformatting, and initiation of a Research Clinics.
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Clinical Studies Center

Informed Consent Review

An Informed Consent Form (ICF) is required for all studies except those granted exempt status by the Emory IRB and must be prepared according to the Emory/VA IRB Consent sample.

Pre-review of the Informed Consent Form is recommended prior to Emory IRB and R&D Committee submission. For ICF review send consent document to the Human Studies Analyst. The preferred format for this document is an e-mail attachment.

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