Processing Checkpoints
        
            During the initial consultation with the Trinity Health Office of Research & Innovation – West Michigan staff, the following topics will be addressed, whether for an investigator initiated study or sponsored clinical trial:
Investigator Initiated Research
- HR clearance
 - Study design development
 - Feasibility/proposal/budget
 - Required agreements
 - Privacy review
 - Data security analysis
 - After all other requirements have been fulfilled, you will be given permission to submit to the Institutional Review Board (IRB)
 
Sponsored Clinical Trial
- Feasibility/proposal/budget
 - Confidentiality Disclosure Agreement (CDA) & Clincal Trial Agreement (CTA)
 - Privacy review
 - Data security analysis
 - After all other requirements have been fulfilled, you will be given permission to submit to the Institutional Review Board (IRB)
 


