Human Subjects

Resource Category Topic Type
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
Guidelines for Research Involving Children/Minors
UNH IRB guidelines for research involving children/minors.
 Compliance & Safety Human Subjects Guidance
Clinical Trial Requirements (NIH)
NIH webpage on clinical trials
 Compliance & Safety Human Subjects Guidance
Privacy, Confidentiality and Anonymity in Human Subjects Research
UNH IRB guidance on privacy, confidentiality and anonymity in human subjects research.
 Compliance & Safety Human Subjects Guidance
Activities Involving Human Subjects and IRB Approval
UNH IRB guidance about activities involving human subjects and UNH IRB approval. Updated December 2024.
 Compliance & Safety Human Subjects Guidance
Payments to Participants, Coercion, & Undue Influence in Human Subjects Research
UNH IRB guidance on payments to participants, coercion, & undue influence in human subjects research.
 Compliance & Safety Human Subjects Guidance
Informed Consent Letter Template (Word version)
Current informed consent letter template (Word version). Updated April 2025.
 Compliance & Safety Human Subjects Form
Informed Consent Document Template (Word version)
Current informed consent document template (Word version). Updated April 2025.
 Compliance & Safety Human Subjects Form
Parent Informed Consent Letter Template (Word version)
Current parent informed consent letter template (Word version). Updated April 2025.
 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 April 2025.
 Compliance & Safety Human Subjects Form