Research
Forms, Templates, and Checklists
This page provides easy access to all the essential forms, checklists, and templates you need to prepare, submit, and manage your research. Whether you're starting a new study or maintaining an ongoing project, these documents are designed to streamline the process, ensure compliance, and support you at every stage of your research.
If you don’t know where to start, visit the Where to Start page or read How to Submit a Research Study to the IRB.
Helpful Documents
- Accounting of Disclosures for <50 Participants
- Accounting of Disclosures for >50 Participants
- Data Use Agreement (DUA)
- Department Approval form
- Financial Interests Disclosure
- HIPAA Authorization - Future Babies
- HIPAA Authorization for Research
- Investigator Agreement
- Materials Transfer Agreement
- Radiation Safety Committee Approval
- Consent Form Template
- Short Form Consent Template - English
- Short Form Consent Template - Spanish
- Consent Form Template - for Compassionate Use of an Investigational Drug
- Protocol Template - for IND/IDE Clinical Trials
- Protocol Template - General
- Assent Form (for use for research with children age 7 and older)
- Reliance Agreement Template
- Required Sponsored Language Checklist
- Checklist for IND Exemption
- Checklist for IDE Criteria
- Checklist for research on pregnant women (45CFR46 subpart B)
- Checklist for research on children (45CFR46 subpart D)
- Checklist for Emergency Use of a Test Article
- ICH checklist for investigators
- Informed Consent Checklist