Key Research Related Policies Research Related Policies IHOP Research Policies Office of Sponsored Programs Grants and Contracts Accounting Office of Clinical Research Animal Resource Center Code of EthicsConduct of Clinical ResearchConsistent Treatment of CostsCost Sharing PolicyCost Transfer PolicyEffort Reporting PolicyEthical Interactions with IndustryExisting Clinical Human Biospecimens Use and TransferExport Control ComplianceForeign Influence in ResearchFringe Benefit CostsGood Clinical Practice (GCP) Training Required for Conducting Clinical TrialsInstitutional Conflicts of InterestInstitutional Office of Regulated Nonclinical StudiesMaintaining Patient Confidentiality through the Appropriate Use and Disclosure of PHIPhotography of Research AnimalsPrincipal Investigator Roles and ResponsibilitiesProcurement PolicyRegistration of Clinical Trials in ClinicalTrials.govResearch Compliance PlanResearch Conflicts of InterestResearch Related Injury of a Subject Participating in a Clinical InvestigationUse & Disclosure of PHI for Research Submission of Applications for Institutional Approvals Resolving Deficits in Sponsored Project AccountsSponsored Award Reconciliation and CloseoutExpense MonitoringClearing Pre-encumbrances and Encumbrances Office of Clinical Research Policies and Standard Operating ProceduresCommunication with SubjectsDetermining Eligibility for Human Subject Research StudiesEpic and OnCore Subject Management ProcessesFDA InspectionObtaining Informed ConsentPre-Screening for Human Subject ResearchPreparation for a Subject VisitReporting Adverse Events/Unanticipated ProblemsResearch SpecimensUTMB Industry Funded Fee Policy ARC Policies and Procedures Research Quick Find Tool Right-Side Nav Research Experts Funding Institutional infoEd OnCore PeopleSoft ECRT