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<V2BodyCopyTray ID="x523215" Name="Definitions" IsComponent="true" Changed="20260416T18:20:18" Created="20260416T17:55:36" Published="20260416T14:04:21" SiteBaseUrl="" Locale="" XPowerPath="/Content Store/home/Policies/Procedures by Category/Compliance and Risk Management Procedures/UWW 730.A: Grant Proposals and Agreements/components/Definitions" Expanded="20260416T17:08:41">
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&lt;p&gt;&lt;strong&gt;Compliance Review:&lt;/strong&gt; Abbreviated review focuses only on areas of proposal submission which, if incorrect, could cause noncompliance such as eligibility issues, F&amp;amp;A calculations, unallowable costs, institutional information, and reportable cost share. It excludes verifying completeness of submission package, formatting requirements, and accuracy of all budget calculations.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Export Control:&lt;/strong&gt; The federal regulations governing the transfer of sensitive technology, software, and data from the U.S. to foreign countries or foreign nationals, even within the U.S.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Institutional Animal Care and Use Committee (IACUC):&lt;/strong&gt; A federally mandated committee that oversees and evaluates an institution's animal care and use program for research, teaching, and testing to ensure the humane and ethical treatment of animals by reviewing and approving research protocols, overseeing animal facilities, and conducting inspections.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Institutional Biosafety Committee (IBC):&lt;/strong&gt; A review board that assesses and approves research involving biohazardous materials, such as recombinant DNA, infectious agents, and toxins to ensure that such research is conducted safely and in compliance with federal guidelines to protect personnel, the public, and the environment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Institutional Review Board for the Protection of Human Subjects (IRB): &lt;/strong&gt;A group that has been formally designated to review and monitor research involving human subjects to protect the rights and welfare of human research subjects, with the authority to approve, require modifications in (to secure approval), or disapprove research.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Post Proposal Actions:&lt;/strong&gt; Materials requested by a sponsor after a proposal has been submitted but prior to an award being made. Examples include sponsor-initiated requests such as progress reports and National Institutes of Health (NIH) Just In Time documents as well as sponsor prior approval requests such as no cost extension requests and budget revisions.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Principal Investigator (PI):&lt;/strong&gt; A Principal Investigator and Co-Principal Investigator are UWW faculty or staff members who bear joint responsibility for the intellectual leadership of a project.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Research Administration Management Portal (RAMP):&lt;/strong&gt; A software solution tailor-made for managing the business of sponsored research, enhancing work in the areas of proposal development and submission, research contracting, non-financial post-award management, employee compensation compliance, and export controls.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Research Security:&lt;/strong&gt; The practice of safeguarding the research enterprise against the misappropriation of research and development, violations of research integrity, and foreign government interference to the detriment of national or economic security.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Technical Narrative:&lt;/strong&gt; The final technical proposal, cited literature, and any component of which the writing is dependent on the science/research/scope of the project.&lt;/p&gt;</BodyCopy>
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