Important Policies that All Investigators Should Read
- HRP-070 Investigator Obligations
- HRP-071 Prompt Reporting Requirements
- HRP-802 Investigator Guidance: Informed Consent
- HRP-803 Investigator Guidance: Documentation of Informed Consent
Below are some frequently used templates/forms that may be included with you ERA submission.
Protocol Templates
Informed Consent Templates
- Main Informed Consent Template
- Minimal Risk Informed Consent Template
- Informed Consent Form for Emergency Use
- Short Form Consent Template
- Survey Interview and Focus Group Consent Template
- Survey and PHI Data Collection Consent Template
- Prospective Chart Review Consent Template
HIPAA Form
Humanitarian Use Device (HUD) Forms
- Application for a HUD 220
- Continuing Review Progress Report or Final Report for a HUD 221
- Modification of an HUD 222
Research Personnel Signature Form: Research Personnel not affiliated with Temple University, Temple University Health System, or Shriner's Hospital for Children should provide their authorization of participation by completing the information below. Include a scanned copy of this document with your IRB submission in ERA.