Study Start-Up Checklist and Forms:
1. Create Protocol (using Intervention Protocol Template)
2. Research Requirements
3. Clinical Research Program (CRP) Feasibility - Submit all documents to CRP@BenaroyaResearch.org
| Device Impact Statement |
Radiology Impact Statement |
| Pharmacy Impact Statement | CRC Impact Statement |
| Nursing Impact Statement | Laboratory/Pathology Impact Statement |
***MUST have feasibility approval before proceeding to Step 4***
4. Submit any Sponsor Clinical Trial Contract / Agreement along with Review Request for negotiations at CTA@BenaroyaResearch.org, if applicable
5. Submit IRB documents to the IRB office at MS: D4-CRP (click here for BRI IRB meeting/deadline schedule)
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***