Below are some frequently used templates/forms that may be included with you ERA submission.

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

Protocol Templates

• Main Protocol Template
• Minimal Risk Protocol Template
• Chart Review Protocol Template

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

• English HIPAA Authorization Form
• Spanish HIPAA Authorization Form
• Spanish Translation Certificate

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: This form is to be used only to collect authorization for Research Personnel who are not affiliated with Temple University, Temple University Health System, or Shriner's Hospital for Children. Affiliated individuals should be added to the ERA system and provide electronic authorization. The PI must always be listed and authorize via ERA, not on this signature form. To add affiliated individuals to ERA, please contact the IRB office at irb@temple.edu or 215-707-3390.

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.