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 [1] for more information about the consent process.
Medical(SoM) [2]
- School of Medicine (SoM)
- Lucile Packard Children's Hospital (LPCH)
- Stanford Hospital and Clinics (SHC)
- Veteran's Affairs (VA) Hospital
- Psychology fMRI studies
Social & Behavioral Research (Non-Medical) [3]
- 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
Protocol Checklists:
- Protocol - Medical [5]
- Protocol - Expedited (initial review) [6]
- Protocol - Chart Review (initial review) [7]
- Protocol - Nonmedical [8]
- Protocol - sIRB Checklist [9]
- VA Research [10]; see Reviewing VA Research [11] for additional requirements
- Exemption from IRB Review: Emergency Use of a Test Article [12]
- Single Patient IND/IDE [13]
Other Federal Agency Requirements:
- Dept. of Defense (DoD) [14]
- Dept. of Education (ED) [15]
- Dept. of Energy (DOE) [16]
- Dept. of Justice (DOJ) [17]
- Environmental Protection Agency (EPA) [18]
Informed Consent:
- Informed Consent [19](medical: clinical studies)
- Informed Consent [20](medical: expedited/minimal risk)
- Informed Consent [21] (nonmedical: surveys, social, behavioral, education research)
- Informed Consent [22] (CIRB)
- Neonates [23]
Continuing Review:
Reviewer Checklists:
- Medical [25]
- Nonmedical [26]