Activities Involving Human Subjects and IRB Approval UNH IRB guidance about activities involving human subjects and UNH IRB approval.
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Compliance & Safety |
Human Subjects |
Guidance |
Clinical Trial Requirements (NIH) NIH webpage on clinical trials
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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.
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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.
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Compliance & Safety |
Human Subjects |
Guidance |
Guidelines for Conducting Survey Research UNH IRB guidelines for conducting survey research. Updated ~ April 2022.
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Compliance & Safety |
Human Subjects |
Guidance |
Guidelines for Human Subjects Research Involving Virtual Reality UNH IRB guidelines on human subjects research involving virtual reality.
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Compliance & Safety |
Human Subjects |
Guidance |
Guidelines for Research Involving Children/Minors UNH IRB guidelines for research involving children/minors. Updated ~ January 2022.
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Compliance & Safety |
Human Subjects |
Guidance |
Guidelines for Research Involving College Students UNH IRB guidance on research involving college students. Updated ~ January 2020.
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Compliance & Safety |
Human Subjects |
Guidance |
Guidelines for Sharing Human Subjects Research Data UNH IRB guidance about sharing human subjects research data. New ~ May 2023.
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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.
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Compliance & Safety |
Human Subjects |
Guidance |
HIPAA Authorization Waiver Request Form UNH IRB HIPAA authorization waiver request form
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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.
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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.
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Compliance & Safety |
Health Insurance Portability & Accountability Act (HIPAA), Human Subjects |
Form |
HIPAA Sample Research Authorization Form UNH IRB HIPAA sample research authorization form.
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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.
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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.
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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.
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Compliance & Safety |
Human Subjects |
Guidance |
Informed Consent Document Template (Word version) Current informed consent document template (Word version) ~ updated January 2022.
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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
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Compliance & Safety |
Human Subjects |
Form |
Informed Consent Format and Checklist UNH IRB guidance on informed consent format and checklist.
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Compliance & Safety |
Human Subjects |
Guidance |