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. New ~ May 2020.
Compliance & Safety Human Subjects Guidance
Guidelines for Research Involving Children/Minors
UNH IRB guidelines for research involving children/minors. Updated ~ January 2020.
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 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
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 May 2021
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 May 2021
Compliance & Safety Human Subjects Form
Informed Consent Format and Checklist
UNH IRB guidance on informed consent format and checklist.
Compliance & Safety Human Subjects Guidance
Informed Consent Letter Template (Word version)
Current informed consent letter template (Word version) ~ updated May 2021
Compliance & Safety Human Subjects Form
Informed Consent Template for a Title IX Reporting Exception for Research form (Word version) ~ updated April 2018
Informed Consent Template for a Title IX Reporting Exception for Research form (Word version) ~ updated April 2018
Compliance & Safety Human Subjects Form
IRB Application Resources
IRB Application Resources
Compliance & Safety Human Subjects Resource