Human Subjects

Resource Category Topic Type
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
HIPAA Sample Research Authorization Form
UNH IRB HIPAA sample research authorization form.
 Compliance & Safety Health Insurance Portability & Accountability Act (HIPAA), Human Subjects Form
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 ~ January 2022.
 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 2022.
 Compliance & Safety Human Subjects Guidance
Activities Involving Human Subjects and IRB Approval
UNH IRB guidance about activities involving human subjects and UNH IRB approval.
 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
Requesting a Modification to a Protocol Previously Approved by the IRB (PDF)
Requesting a modification to a protocol previously approved by the UNH IRB (PDF)
 Compliance & Safety Human Subjects Form