Forms & Consent Templates

Consent Templates

The IRB recommends the use of the consent templates to help researchers meet the legal requirements for consent.

See the Informed Consent Process page for more information about the consent process.  

Medical (SoM)

• School of Medicine (SoM)
• Stanford Medicine Children’s Health (SMCH)
• Stanford Medicine Health Care (SMHC)
• Veteran's Affairs (VA) Hospital
• Psychology fMRI studies

Social & Behavioral Research (Non-Medical)

• Business
• Education
• Engineering
• Humanities & Sciences
• Law

Checklists

The IRB uses these checklists and forms to review protocols for compliance with regulations, policies and guidance:

Staff Checklists

• Exemption Eligibility

 Protocol Checklists:

• Protocol - Medical
• Protocol - Expedited (initial review)
• Protocol - Chart Review (initial review)
• Protocol - Nonmedical
• Protocol - sIRB Checklist
• SCRO Renewal Review Checklist
• Research Involving VA Studies; see Reviewing Veterans Affairs (VA) Research for additional requirements
• Exemption from IRB Review: Emergency Use of a Test Article
• Single Patient IND/IDE

Other Federal Agency Requirements:

• Dept. of Defense (DoD)
• Dept. of Education (ED)
• Dept. of Energy (DOE)
• Dept. of Justice (DOJ)
• Environmental Protection Agency (EPA)

Informed Consent:

• Informed Consent (medical: clinical studies)
• Informed Consent (medical: expedited/minimal risk)
• Informed Consent (nonmedical: surveys, social, behavioral, education research)
• Neonates

Continuing Review:

• Continuing Review - FULL/EXPEDITED

Reviewer Checklists:

• Medical
• Nonmedical