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Allina Health Research Administration

  • Allina Health Research Administration

    Allina Health Research Administration assists researchers in meeting regulatory obligations in the areas of human research protections, HIPAA privacy in research, research billing, and the financial management of grants and contracts.

    We are comprised of three areas:

    • The Human Research Protection Program (HRPP) and its Institutional Review Boards (IRBs) protect the rights and welfare of subjects who participate in human subjects research conducted in Allina Health facilities or by Allina Health employees or agents. Designated IRBs provide review and ongoing oversight of human subjects research.
    • The Office of Sponsored Programs (OSP) is responsible for research billing compliance, the financial management of government grants and other sponsored project funds award to Allina Health.
    • The Clinical Research Informatics and Analytics (CRIA) team is composed of staff with expertise in health informatics, project management, data extraction and report writing, and statistics. CRIA collaborates with various teams at Allina Health to provide comprehensive research support services related to research data access, use, and disclosure.
  • New to research at Allina Health?

    Your project may require prior approval. All research conducted at an Allina Health facility and/or by Allina Health employees or agents must follow applicable policies and procedures.

     Answers to theses questions will help determine whether your project requires prior approval from the Human Research Protections Program (HRPP) and/or Office of Sponsored Programs.

    Are you conducting research on or with human subjects or their information?

    Will the research project use Allina Health facilities for any items or services related to an investigational drug or device?


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