Forms and Guidance

Adjunct Faculty Request to Serve as PI

• Adjunct Faculty Request to Serve as PI

Adult Consent Templates

• Simplified Consent Form Template
• Additional Language for Simplified Consent Form Template
• Comprehensive Consent Form Template
• Addendum to the Informed Consent Form New Information for Continuing Research Participants – Template
• Broad Consent for Future Research Uses of Identifiable Private Information and or Identifiable Biospecimens
• Deception Debriefing Form

Parent Permission Templates

• Simplified Parent Permission Form Template
• Additional Language for Simplified Parent Permission Form Template
• Comprehensive Parent Permission Template

Child Assent Templates

• Child 3-6 Assent Script Template
• Child 7-12 Assent Form Template
• Simplified Combined Permission Assent Template (Ages 13-17 only)
• Comprehensive Combined Permission Assent Template (Ages 13-17 only)

General

• 2CUNY HRPP Informed Consent Process and Documentation Tip Sheet
• Accounting for Total Subject Enrollment
• CITI Training in the Protection of Human Subjects
• Faculty Advisor or Research Program Manager Responsibilities
• HRPP Staff Responsibilities
• Informed Consent Process and Documentation
• IRB Appeals Process
• IRB Member Roles and Responsibilities
• IRB Membership
• Principal Investigator Qualifications and Responsibilities
• Researcher Responsibilities
• Student Subject Pools
• Study Closures
• Suggested Language for Consent Documents
• Suspension or Termination of Human Subject Research
• When is CUNY HRPP or IRB Review Required?

IRB Review

• Convened IRB Review
• Criteria for IRB Approval
• CUNY UI-IRB Authority
• Expedited Review of Human Subjects Research
• Human Subjects Research Exempt from IRB Review
• Limited IRB Review

Non-compliance and Reporting

• Disposition of Allegations of Non-Compliance
• Submission Flow Chart: Unanticipated Problems and Adverse Events
• tDCS Adverse Event Reporting Form
• TMS Adverse Event Reporting Form
• TMS and tDCS Adverse Event Monitoring Requirement
• Unanticipated Problems and Adverse Events

Study-specific

• Children as Research Subjects
• Definitions and Requirements for Clinical Research, Clinical Trials and Clinical Investigations
• Department of Defense Conducted or Supported Research
• FDA Regulated Research
• FERPA Compliance: Requesting and Using Data from CUNY Educational Records for Research Purposes
• GDPR Compliance: Collecting Personal Data About Individuals within the European Economic Area (EEA)
• Guidance for Studies Obtaining Information on Suicidal Ideation or Suicide Attempts
• Internet or Mobile Technology Based Research
• Mandated Reporting in the State of New York
• MRI Standard Language for IRB Protocols
• Non-Exempt Cooperative Human Subject Research
• Pregnant Women, Human Fetuses and Neonates as Research Subjects
• Prisoners as Research Subjects
• Recruitment of Students as Research Subjects
• Research Conducted in an International Setting
• Research Funds Memo
• Resource for CUNY Researchers doing research in or about New York City Public Schools
• Secondary Research Use of Identifiable Private Information or Identifiable Biospecimens
• Use of Raffles as Compensation for Participation

Data Classification and Information Security

• CUNY Policy on Acceptable Use of Digital Assets and Resources
• IT Security Procedures – Acceptable Use of University Data in the Cloud
• IT Security Procedures – Data Classification Standard