Investigator-Initiated Trial Agreement Template

6. Submit a study summary that will be published on the BRI website by contacting us at MUST have a feasibility authorization before proceeding with step 4***5. All new applications must be submitted by eProtocol. Please see the IRB page for more instructions. 4. Submit a contract/agreement for the sponsor`s clinical trial as well as a request for review for negotiations with, if applicable (approximately 8-16 weeks between filing and registration) 1. Create Protocol [using Intervention Protocol Template (option 1) or ITHS Intervention protocol template (option 2) ****CRP “Letter to Commence” MUST be received, Before a study activity can take place**** 3. Clinical Research Program (CRP) Feasibility – Submit all documents to . .


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