Human Subjects

Resource Category Topic Type
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 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. Updated April 2026.
 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. Updated April 2026.
 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 2026.
 Compliance & Safety Human Subjects Form
Informed Consent Document Template (Word version)
Current informed consent document template (Word version). Updated April 2026.
 Compliance & Safety Human Subjects Form
Parent Informed Consent Letter Template (Word version)
Current parent informed consent letter template (Word version). Updated April 2026.
 Compliance & Safety Human Subjects Form