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Evidence-Based Practice Nursing Toolkit

Tools and Resources

Henry Ford Health Requirements for Principal Investigators (PIs):

  • The Henry Ford Health Institutional Review Board (IRB) must prospectively review investigational studies that involve human subjects in an experimental or observational context. PIs and those directly involved in the research process must complete the appropriate training modules prior to initiating human subjects research 
  • IRB training requirements are dependent on the type of research being planned. Detailed information is available at Research Administration via the link: Institutional Review Board
  • Recommended CITI program courses are the Good Clinical Practice CITI training modules 
  • The IRB New Protocol Submission Form can be completed once CITI training is done and the New Protocol Submission Form is complete: IRB Application Forms

The HFH Center for Nursing Research and EBP (CNRE) and clinical nurse specialists can assist with the IRB application process 

Points to Ponder

To-Do's

Consult with Public Health Sciences before IRB submission to determine how many participants should be included in your study to demonstrate an effect from your practice change  (313-874-6360, OFP-3)
Prior to IRB submission, request a review of the application by the HFH Center for Nursing Research and EBP (CNRE)
Following application signoff by the CNRE and prior to submission, the application must be signed by the PI and the HFH CNO or System CNO.
Submit the IRB application to HFHS IRB review board. (approximately 4 weeks is required for expedited reviews)