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The CCTS's Biomedical Informatics Core manages the Clinical Research Data Warehouse. Campus investigators can work with Biomedical Informatics specialists to gain access to the warehouse and obtain both data counts and data extracts.

VIReC develops resources for and provides guidance to VA researchers using VA data. Their mission is to improve the quality of VA research that utilizes databases and information systems.

SRL has offices on the Chicago and Urbana-Champaign campuses of the University and can undertake complete survey projects from initial study design through data analysis. It also can conduct partial survey work and provide consultation on survey problems on a fee-for-service basis.

Established in 1997, Community-Campus Partnerships for Health (CCPH) is a nonprofit membership organization that promotes health equity and social justice through partnerships between communities and academic institutions.

The NIH Office of Extramural Research provides of listing of policies,regulations and guidance on reseach involving human subjects.

Bioethics Resources on the Web provides a compilation of web links to information of potential use and interest to diverse audiences—biomedical and behavioral researchers, health care professionals, research participants, patients and patient advocates, students and faculty in different disciplines, and the general public.

The UIC Environmental Health and Safety Office (EHSO) provides the university's policies and procedures on a variety of safety issues.

UIC provides bloodborne pathogen training through the online Exposure Control Plan provided by the Environmental Health and Safety Office.

ORS assists faculty and staff in proposal development, review and endorsement of proposals, submission of electronic proposals, negotiation and execution of contracts, reporting, receipt and processing of the Notice of Awards (NOA), interpretation of sponsor guidelines, and ensuring compliance with both agency and University policies.

The Centers for Disease Control and Prevention provide information on human participant protection in clinical investigations involving human subjects and the use of drugs, biologics or devices.

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