(approx. 4 weeks from submission to enrollment)

Study Start-Up Checklist and Forms:

1. Create Protocol - Non Interventional Chart Review Template

• Mentor/Unit Director should review draft of protocol

2. Research Requirements

Submit Request for IRB  Number form, if applicable (include all Key Personnel)

• Complete Good Clinical Practices Training (all key personnel)
• Complete Ethics Training (all key personnel)
  
• Submit BRI / Investigator Compact (for investigators new to research or new to VMMC)

3. Clinical Research Program (CRP) Feasibility - Submit all documents to CRP@BenaroyaResearch.org

• Database / Data Collection Form (if applicable)
  
• Chart Review Protocol
  

***MUST have feasibility approval before proceeding to Step 4***

5. Submit Institutional Review Board (IRB) documents to the IRB office at MS: D4-CRP.

• Institutional Review Board Application Cover Sheet
• Chart Review Application. Please contact Unit Manager for more information.

For additional assistance, contact the IRB at IRB@BenaroyaResearch.org

6.Submit study synopsis to appear on BRI website

***CRP "Letter to Commence” MUST be received before any study activity can occur***