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IRB Library

The IRB Library houses submission documents, guidance, and policies for the research community to access and download.

  • Forms - IRB application documents
  • Templates - sample documents for an IRB submission
  • Guidance - information on important topics such as FERPA and data security
  • Policies - standard operating procedures (SOPs) for the review of human subjects research
  • PAM - post approval monitoring, documents to assist researchers with ongoing monitoring of research
Document Category Document File Document Description Version Date
Policies PDF icon 308.0 Review of FDA Regulated Drugs and Devices When FDA regulations apply and review of FDA regulated research 01/30/2019
Guidance PDF icon FDA Regulated Drugs and Devices Researcher responsibilities for research with drugs or devices 06/04/2019