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UIUC Institutional Review Board - University of Illinois - IRB Administration

Part I: Research Subject to IRB Review. Part II: Fundamental Guidelines. Part III: Distribution of Responsibility. Part IV: Review Procedures. Part V: Special Subject Groups. Human Subjects Research Defined. Research Equipment Form, App A. Drugs and Devices Form, App B. Biological Materials Form, App C. Informed Consent Related Waivers. Sample List of Local Referrals. Food, Drug Administration. Office for Human Research Protections. Elements of Informed Consent. Pregnant Women, Fetuses, Neonates.

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UIUC Institutional Review Board - University of Illinois - IRB Administration | oprs.research.illinois.edu Reviews
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Part I: Research Subject to IRB Review. Part II: Fundamental Guidelines. Part III: Distribution of Responsibility. Part IV: Review Procedures. Part V: Special Subject Groups. Human Subjects Research Defined. Research Equipment Form, App A. Drugs and Devices Form, App B. Biological Materials Form, App C. Informed Consent Related Waivers. Sample List of Local Referrals. Food, Drug Administration. Office for Human Research Protections. Elements of Informed Consent. Pregnant Women, Fetuses, Neonates.
<META>
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1 investigator handbook
2 contents
3 glossary of terms
4 irb administration
5 introduction
6 irb membership
7 irb office
8 review procedure
9 exempt research
10 expedited review
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investigator handbook,contents,glossary of terms,irb administration,introduction,irb membership,irb office,review procedure,exempt research,expedited review,continuing review,federalwide assurance,forms and instructions,initial irb 1 application,tipsheet
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UIUC Institutional Review Board - University of Illinois - IRB Administration | oprs.research.illinois.edu Reviews

https://oprs.research.illinois.edu

Part I: Research Subject to IRB Review. Part II: Fundamental Guidelines. Part III: Distribution of Responsibility. Part IV: Review Procedures. Part V: Special Subject Groups. Human Subjects Research Defined. Research Equipment Form, App A. Drugs and Devices Form, App B. Biological Materials Form, App C. Informed Consent Related Waivers. Sample List of Local Referrals. Food, Drug Administration. Office for Human Research Protections. Elements of Informed Consent. Pregnant Women, Fetuses, Neonates.

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research.illinois.edu research.illinois.edu

Regulatory Compliance & Safety | Office of the Vice Chancellor for Research

http://research.illinois.edu/regulatory-compliance-safety

Skip to main content. Office of the Vice Chancellor for. University of Illinois at Urbana-Champaign. About the Illinois Research Enterprise. Research Centers and Programs. Resources for Research Overview. Find Facilities, Labs, and Services. Find Proposal and Grant Support. Support for Grantseeking in the Humanities, Arts, and Social Sciences. Business Policies and Guidelines. Business Policies and Guidelines Overview. OVCR Cost Sharing Guidelines. Regulatory Compliance and Safety. Animal Care and Use.

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UIUC Institutional Review Board - University of Illinois - IRB Administration

Part I: Research Subject to IRB Review. Part II: Fundamental Guidelines. Part III: Distribution of Responsibility. Part IV: Review Procedures. Part V: Special Subject Groups. Human Subjects Research Defined. Research Equipment Form, App A. Drugs and Devices Form, App B. Biological Materials Form, App C. Informed Consent Related Waivers. Sample List of Local Referrals. Food, Drug Administration. Office for Human Research Protections. Elements of Informed Consent. Pregnant Women, Fetuses, Neonates.

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