Investigator-Initiated Trial Agreement Template

5. All new applications for studies must be submitted to the electronic protocol. For more information, visit the IRB page. 3. Clinical Research Program (CRP) Feasibility – Submit all documents to “Letter to The Beginning” MUST be received before a study activity can take place – MUST have a feasibility permit before proceeding to Stage 4-6. Present a summary of the study, which will be published on the BIS website by contacting us at 1. Create a protocol [with Intervention Protocol Template (Option 1) or ITHS Interventional Protocol Template (Option 2)] (about 8 to 16 weeks from transmission to recording) 4. Send, if necessary, a clinical testing procedure contract or agree with a review request for negotiations with