Category: Human Subjects

Resource Category Topic Type
Activities Involving Human Subjects and IRB Approval
UNH IRB guidance about activities involving human subjects and UNH IRB approval.
 Compliance & Safety Human Subjects Guidance
Clinical Trial Requirements (NIH)
NIH webpage on clinical trials
 Compliance & Safety Human Subjects Guidance
Ethical Use and Treatment of Human Subjects in Research Web-based Instruction
UNH Ethical Use and Treatment of Human Subjects in Research Web-based Instruction.
 Compliance & Safety Human Subjects Instruction & Training
European Union (EU) General Data Protection Regulation (GDPR) & Human Subjects Research
UNH IRB guidance on the European Union's (EU) General Data Protection Regulation (GDPR) and human subjects research.
 Compliance & Safety Human Subjects Guidance
Guidelines for Conducting Survey Research
UNH IRB guidelines for conducting survey research. Updated ~ April 2022.
 Compliance & Safety Human Subjects Guidance
Guidelines for Human Subjects Research Involving Virtual Reality
UNH IRB guidelines on human subjects research involving virtual reality.
 Compliance & Safety Human Subjects Guidance
Guidelines for Research Involving Children/Minors
UNH IRB guidelines for research involving children/minors. Updated ~ January 2022.
 Compliance & Safety Human Subjects Guidance
Guidelines for Research Involving College Students
UNH IRB guidance on research involving college students. Updated ~ January 2020.
 Compliance & Safety Human Subjects Guidance
Guidelines for Sharing Human Subjects Research Data
UNH IRB guidance about sharing human subjects research data. New ~ May 2023.
 Compliance & Safety Human Subjects Guidance
Guidelines for Use of External IRBs and Single IRBs
UNH IRB guidance on the use of external IRBs and single IRBs.
Compliance & Safety Human Subjects Guidance
HIPAA Authorization Waiver Request Form
UNH IRB HIPAA authorization waiver request form
 Compliance & Safety Health Insurance Portability & Accountability Act (HIPAA), Human Subjects Form
HIPAA Impacts on Research Involving Human Subjects
UNH IRB guidance on HIPAA impacts on research Involving human subjects.
 Compliance & Safety Health Insurance Portability & Accountability Act (HIPAA), Human Subjects Guidance
HIPAA Sample Authorization Language for Consent Forms
UNH IRB HIPAA sample authorization language for consent forms.
 Compliance & Safety Health Insurance Portability & Accountability Act (HIPAA), Human Subjects Form
HIPAA Sample Research Authorization Form
UNH IRB HIPAA sample research authorization form.
 Compliance & Safety Health Insurance Portability & Accountability Act (HIPAA), Human Subjects Form
Human Subject Incentive Payments
To provide guidance for the payment of incentives to human subjects participating in research projects, and to determine when the gathering of research participant tax information is required.
Award/Funding Management Human Subjects Resource
Individual Investigator Agreement
An agreement to involve in a study involving human subjects non-UNH investigators who are consultants or who are not affiliated with an organization that has an IRB.
 Compliance & Safety Human Subjects Form
Information Individuals in New Hampshire are Legally Required to Report
UNH IRB guidance on information individuals in New Hampshire are legally required to report.
 Compliance & Safety Human Subjects Guidance
Informed Consent Document Template (Word version)
Current informed consent document template (Word version) ~ updated January 2022.
 Compliance & Safety Human Subjects Form
Informed Consent Document Template for Studies Using the Psychology Department Subject Pool (Word version)
Current informed consent document template for studies using the Psychology department subject pool (Word version) ~ updated January 2022
 Compliance & Safety Human Subjects Form
Informed Consent Format and Checklist
UNH IRB guidance on informed consent format and checklist.
 Compliance & Safety Human Subjects Guidance