Forms and Templates
New Study Initial Review Submission Documents
- Clinical Trials Office Research Application (Required for all submissions)
- Request for Waiver of Informed Consent or Elements of Informed Consent
Templates
Protocol
Informed Consent Document
- INFORMED CONSENT AND AUTHORIZATION TO PARTICIPATE IN RESEARCH (Adult)
- Revocation Letter Template
- Social Behavioral Consent Document Template
Assent Document
- Assent Template (Children)
HIPAA Document
Reportable Events
- UMC IRB Guidance Investigator Reporting Obligations – version 1, dated 06/2015
- UMC Sample Reportable Event Summary – version 1, dated 06/2015
- Reportable Events Assessment Tool dated 06/18/2015
Conflict of Interest
Permanent Closure of Research Protocol
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