Forms and Templates
New Study Initial Review Submission Documents
- Clinical Trials Office Research Application (Required for submissions that have billable items and/or services)
Data Requests for Research
- All requests for research data from UMC require that a Service Request be submitted through: https://itservices.umcsn.com/
- All requests must include the UMC IRB approval letter and a completed Report/Data Request Form
Templates
Protocol
- Biomedical Protocol Template
- Social Behavioral Protocol Template
- Chart Review Protocol Template
- Retrospective Chart Review Application Sample
Informed Consent Document
Assent Document
- Assent Template (Children)
HIPAA Document
Data Collection Tools
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
This translation is provided by Google Translate. University Medical Center of Southern Nevada makes no representations or warranties of any kind, whether express or implied, regarding the accuracy of the translation provided above.