№ lp_1_2_42079
Guidelines for preparing and submitting clinical research protocols, consent documents, and regulatory materials to the IRB for review and approval.
Year: 2026
Institution: University of Chicago
Document Type: Submission Guidelines
Audience: Principal Investigators, Clinical Researchers
Related Regulations: CR_Policy 110, FDA regulations
Submission Platform: AURA-IRB
Required Documents: Protocol narrative, consent forms, IB/drug information, device manuals, PRMC approval if applicable
Funding: External or internal funding sources noted
Resubmission: Response to prior IRB comments if applicable
Price: 8 / 10 USD
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