Research@UIC > Protocol Review > IRB > Getting Started

Getting Started

A Guide for Investigators and Research Staff                 

What is human subjects research? What is research? What are human subjects? Examples of Human Subjects Research Who is required to submit an IRB application? Who must be included on my protocol? What types of training is required for investigators and Key Research Personnel? What is the Role of the UIC Institutional Review Board (IRB)? What are the types of protocol review? Decision Tree for Submitting Medical Record Review Research What about the VA? What is informed consent? Top Ten Tips Helpful links

Helpful links

U.S. Department of Health and Human Services (DHHS)

• Office for Human Research Protections (OHRP)

• U.S. Food and Drug Administration (FDA)

U.S. Department of Education                    

• http://www.ed.gov

University of Illinios at Chicago

• RiSCWeb
  • Look up the status of your protocol
  • Download OPRS correspondence
  • Designate protocol access
  • View your training record
  • View IRB meeting & submission Date

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Last updated: Friday, September 18, 2009.