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
Classroom Practica Form
Other forms
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