Templates & »Æ¹ÏÊÓƵ
Templates & »Æ¹ÏÊÓƵ
Templates & Samples
Supporting Documents
- Faculty Advisor Review Form
- Individual Investigator Agreement (IIA) Form
- DoD Funded Research: Scientific Merit Review Letter
- International Research: Foreign Local Review Letter
Guidance DocumentsÌý
- International Research (EU/EEA): General Data Protection Regulation (GDPR)
- FDA Device Regulations: Investigational Device Studies
- Data Security
- Deception and Incomplete Disclosure
- Focus Group
- Research in K-12 Schools
- Students as Research Subjects: How to Avoid Undue Influence and Coercion
- Classroom Research Projects
- Research Involving Marijuana/Cannabis
- Protocol Standards and Language for Studies Involving MRI
- Determining and Reporting Adverse Events
Additional Information & Regulatory Links
- Exempt ResearchÌý ÌýÌý
- Single IRB
- IRB Investigator Manual ÌýÌý
- IRB Board Meeting ScheduleÌýÌý
- CU Boulder IRB PoliciesÌýÌýÌý
- The Belmont Report: The document that summarizes the basic ethical principles of research.
- : Comprehensive information regarding the federal regulations.
- : HHS agency that regulates clinical investigations products under its jurisdiction (drugs/biological products/medical devices).
- : Information from the Department of Health and Human Services on protecting human subjects in research.
- : Conditions under which protected health information may be used or disclosed by covered entities for research purposes.
- : A list of international agencies that oversee human subject research protections
- : An collection of informational resources pertaining to bioethics and biomedical research.
- : A graphic aid to help you decide if your research must be reviewed by the IRB.
Research and expertise across CUÌýBoulder.
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Our 12Ìýresearch institutes conduct more than half of
the sponsored research at CUÌýBoulder.
More than 75 research centers span the campus,
covering a broad range of topics.
A carefully integrated cyberinfrastructure supports CUÌýBoulder research.
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