Forms and Guidance
Consent Forms
- Addendum to the Informed Consent Form New Information for Continuing Research Participants – Template
- Adolescent (Age 13-17) Assent Parental Permission For Child (Age 13-17) to Participate in a Research Study – Template
- Broad Consent for Future Research Uses of Identifiable Private Information andor Identifiable Biospecimens
- Child Assent (Ages 7-12) to Participate in a Research Study – Template
- Consent to Participate in a Research Study – Template
- Deception Debriefing Form
- Informational Sheet for Exempt Studies
- Oral and Internet-Based Informed Consent Script Template
- Parental Permission For Child (Age up to 12) to Participate in a Research Study – Template
- Required Informed Consent Language for Studies Using MRI Procedures
- Required Language for Studies Where the GDPR Applies
Faculty Classroom Practica Form
Request to Recruit Participants for Research Form
Adjunct Faculty Request to Serve as PI
Guidance, Policies, and Procedures
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