University of Cincinnati Office of Research

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77 search results for Research Security

Techonology Control Plan (PDF)

The Technology Control Plan (TCP) details the established measures to ensure compliance with the U.S. regulations by the principal investigator/responsible individual.

Contact Office: ExportControl

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1.3.2 Conflict of Interest on Externally Funded Projects (PDF)

The purpose of this policy is to assure that the objectivity and integrity of the researcher, the University of Cincinnati (UC), and academic research, training, or other activities are not compromised or perceived to be compromised by matters of financial benefit or personal gain.
The policy provides the university’s approach to identifying individual financial relationships, evaluating, and determining potential financial conflicts of interest related to research activities as well as developing strategies to manage conflicts. This policy assists faculty, staff, and students in meeting their obligations to conduct research responsibly, ethically, and objectively and to comply with applicable federal, state, and local regulations and university rules and policies.

Contact Office: RSE

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Genetics Consent with HIPAA Language (DOCX)

The Genetics Informed Consent Statement is to be used in the following cases:

  1. When the investigator is conducting genetic research on blood or tissue acquired from known subjects (one consent form).
  2. When the investigator is conducting genetic research as a sub-study within another study and the participation in the genetic research is optional (two consent forms for those who participate, one for those who do not).
  3. When the investigator is conducting genetic research as a sub-study within another study, but the participation in the genetic research is not optional, incorporate the additional elements in the genetics consent form into the primary informed consent statement (one consent form).

Contact Office: HRPP

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Recruitment and Study Related Materials Guide (PDF)

Advertisements, recruitment materials and study-related materials are an extension of the informed consent process.  The UC IRB reviews recruitment and study-related materials according to federal regulations [both Department of Health and Human Services (DHHS) and Food and Drug Administration (FDA) ], International Conference on Harmonization (ICH) Guidelines (if applicable) and the Board’s policies and procedures. These regulations and guidelines require that Institutional Review Boards (IRBs)] make sure that the selection of participants for a study is equitable.

Contact Office: HRPP

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Foreign Travel Briefing & Acknowledgement (PDF)

This form contains information for any UC faculty, staff, or student that will be traveling to a sanctioned or embargoed country on behalf of the university.  This form is to be used in conjunction with the International Travel Certification form if traveling with UC owned property.

Contact Office: ExportControl

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Quality Management Program for Researchers (PDF)

This program is established to provide high confidence that radiation from radioactive material will be administered to human research subjects as directed by the Human-use Authorized User as authorized by the Radiation Safety Committee under the Radiation Control and Safety Program of the University of Cincinnati.

Contact Office: RadSafety

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Genetics Consent (DOCX)

The Genetics Informed Consent Statement is to be used in the following cases:

  1. When the investigator is conducting genetic research on blood or tissue acquired from known subjects (one consent form).
  2. When the investigator is conducting genetic research as a sub-study within another study and the participation in the genetic research is optional (two consent forms for those who participate, one for those who do not).
  3. When the investigator is conducting genetic research as a sub-study within another study, but the participation in the genetic research is not optional, incorporate the additional elements in the genetics consent form into the primary informed consent statement (one consent form).

Contact Office: HRPP

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Primer on Facilities and Administrative Costs (PDF)

This Primer is designed to provide background information about Facilities and Administrative (F&A) costs to members of the University of Cincinnati community. It begins with a brief history of F&A cost funding, then describes how F&A cost rates are calculated, defines the various cost components used to calculate an institutional rate, and explains how F&A cost recovery provides significant funding for the infrastructure and administrative activities necessary to carry out the University's research programs.

Contact Office: GCC

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