Humanitarian Device Trials

(approx 4 - 6 weeks from submission to enrollment)

Study Start-Up Checklist and Forms:

1. Research Requirements.

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

Device Impact Statement
          Radiology Impact Statement
Nursing Impact Statement          

CRC Impact Statement
CRC Med Order Sample
CRC FAQ's

Laboratory/Pathology Impact Statement          

***MUST have feasibility approval before proceeding to Step 3***

3. Submit Clinical Trial Contract/Agreement Review Request to CTA@BenaroyaResearch.org (if applicable).

4. Submit Institutional Review Board (IRB) documents for review and approval. Industry studies will be submitted electronically to Western IRB (WIRB) via BRI IRB at IRB@benaroyaresearch.org:

Simultaneous approval can occur if preauthorization of WIRB submission is granted.

5. Enter study into CTMS ONLY if a budget is required.

6. Submit study synopsis to appear on BRI website


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