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The UNH Research Office Knowledge Base is designed expressly to support UNH faculty and graduate researchers throughout the research development life cycle. Use the filter tools below to access forms, instruction and training material, committee minutes, policies, tools and other resources to support your research efforts by topic area.
If you are unsure of the Type/Category/Topic please choose -Any-
| Resource | Category | Topic | Type |
|---|---|---|---|
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UNH IRB guidance about activities involving human subjects and UNH IRB approval.
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Compliance & Safety | Human Subjects | Guidance |
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UNH IRB application form for a Title IX reporting exception for research (fillable PDF version).
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Compliance & Safety | Human Subjects | Form |
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UNH IRB application form for a Title IX reporting exception for research (Word version)
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Compliance & Safety | Human Subjects | Form |
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Application materials for UNH IRB review (Fillable PDF) ~ updated January 2018
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Compliance & Safety | Human Subjects | Form |
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Application materials for UNH IRB review (RTF version) ~ updated January 2018
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Compliance & Safety | Human Subjects | Form |
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Application materials for UNH IRB review (Word version) ~ updated January 2018
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Compliance & Safety | Human Subjects | Form |
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NIH webpage on clinical trials
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Compliance & Safety | Human Subjects | Guidance |
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UNH Ethical Use and Treatment of Human Subjects in Research Web-based Instruction.
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Compliance & Safety | Human Subjects | Instruction & Training |
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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 |
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UNH IRB guidelines for conducting survey research. New ~ May 2020.
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Compliance & Safety | Human Subjects | Guidance |
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UNH IRB guidelines for research involving children/minors. Updated ~ January 2020.
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Compliance & Safety | Human Subjects | Guidance |
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UNH IRB guidance on research involving college students. Updated ~ January 2020.
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Compliance & Safety | Human Subjects | Guidance |
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UNH IRB guidance on the use of external IRBs and single IRBs.
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Compliance & Safety | Human Subjects | Guidance |
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UNH IRB HIPAA authorization waiver request form
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Compliance & Safety | Health Insurance Portability & Accountability Act (HIPAA), Human Subjects | Form |
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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 |
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UNH IRB HIPAA sample authorization language for consent forms.
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Compliance & Safety | Health Insurance Portability & Accountability Act (HIPAA), Human Subjects | Form |
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UNH IRB HIPAA sample research authorization form.
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Compliance & Safety | Health Insurance Portability & Accountability Act (HIPAA), Human Subjects | Form |
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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 |
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UNH IRB guidance on information individuals in New Hampshire are legally required to report.
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Compliance & Safety | Human Subjects | Guidance |
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Informed consent document template (RTF version) ~ updated May 2018.
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Compliance & Safety | Human Subjects | Form |