Forms & Guidance
Standard Operating Procedures (SOPs)
- All SOPs (full document)
- Human Research Protections Program
- The Institutional Review Board
- The IRB Review Process
- Documentation and Records
- Obtaining and Documenting Informed Consent from Research Participants
- Quality Assurance: Post-approval Monitoring of Approved Human Subject Research
- Unanticipated Problems Involving Risks to Participants and Others, Complaints, Noncompliance and Suspension or Termination of IRB Approval of Research
- Vulnerable Populations
- Human Research Protections Program
Guidance
Announcements
- No current announcements
CITI Training
Consent
- Language for Child Assent (under age 12)
- Language for Consent Forms
- Language for Parental Permission Forms
- Consent Form Generator
GDPR
Cooperative Research - Guidance and Reliance Request Forms
- Form 1: Request another institution to rely on the NYU IRB
- Form 2: Request for NYU to rely on another IRB
- Form 3: Request for an independent investigator to rely on the NYU IRB
- Single IRB for Federal Common Rule Agencies
Other
- Applying to the NYU IRB as a Student
- Guidance for Faculty Sponsors
- IRB Decision Tree
- Letter of Collaboration Template
- Prisoner Guidance
- NIH Data Sharing Requiring GUIDs
- Not Human Subjects Checklist
- NYU Federalwide Assurance
- Quality Assurance: Post-Approval Monitoring
- Research Expenditures Involving Participant Support Costs and Human Subject Payments (FAQs)
- Single IRB (sIRB)
- Submission Deadlines for Full Board Applications
- Title IX Reporting Exception for Human Subjects Research
- Undergraduate Student (Classroom) Research