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The University of Michigan Office of Research (UMOR) has central responsibility for nurturing excellence in research, scholarship and creative activity across the entire campus. Limited Submission and other funding competitions are managed by the Office of Vice President for Research (OVPR).

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UMOR is home to a variety of diverse interdisciplinary research units that span topics ranging from human development to energy to mobility transformation, and research units like the Business Engagement Center (BEC) and TechTransfer.

ORSP manages pre-award and some post-award research activity for U-M. We review contracts for sponsored projects applying regulatory, statutory and organizational knowledge to balance the university's mission, the sponsor's objectives, and the investigator's intellectual pursuits.

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Ethics and compliance in research covers a broad range of activity from general guidelines about conducting research responsibly to specific regulations governing a type of research (e.g., human subjects research, export controls, conflict of interest).

eResearch is U-M's site for electronic research administration. Access: Regulatory Management (for IRB or IBC rDNA applications); Proposal Management (eRPM) for the e-routing, approval, and submission of proposals (PAFs) and Unfunded Agreements (UFAs) to external entities); and Animal Management (for IACUC protocols and ULAM).

Sponsored Programs manages the post-award financial activities of U-M's research enterprise and other sponsored activities to ensure compliance with applicable federal, state, and local laws as well as sponsor regulations. The Office of Contract Administration (OCA) is also part of the Office of Finance - Sponsored Programs.

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Research Ethics & Compliance
Compliance Hotline

Ethics & Compliance

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        • Waivers of Informed Consent Guidelines
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  • Research Safety
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    • Institutional Biosafety Committee (IBC)
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      • Requirements for rDNA and SNA Research
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        • FAQs: Types of Potentially Hazardous Biological Materials Page
        • Instructions: Adding Work with LPS
      • Human Gene Transfer Clinical Trials
      • IBC Meetings and Submission Deadlines
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      • Reporting Safety Incidents Involving Potentially Hazardous Biologics
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  • Research Integrity
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    • Office of Research Compliance Review (ORCR)
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      • Self-Assessment Tools
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    • Responsible Conduct of Research (RCR) Training
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  • Conflict of Interest
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    • COI Policies
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    • Principles & Concepts
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      • U-M Start-Up Company Disclosure Process
      • M-Inform Glossary & FAQ
    • COI Initial Review Process
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  • Export Controls
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    • Restricted Party Screening
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    • Joint Certification Program: U.S. - Canada
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  • Research Information Security
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    • Controlled Unclassified Information (CUI)
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