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Investigators often request language to describe the CCTS and/or a specific service or resource for inclusion in a grant application. The CCTS Overview and Service Core Description provides the necessary information for most applications.

This PowerPoint presentation will provide UIC study coordinators with an overview of campus laboratory testing services, policies and procedures.

The Request for Use of University Hospitals and Clinic Services form is required for investigators who wish to use hospital or clinic technical services as part of a clinical trial.

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.

Clinical Research Boot Camp is an intensive 3-day training program tailored to meet the specific needs of clinical research personnel and teach them to carry out successful clinical research studies.

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.

Community Engaged Research Boot Camp an intensive, 3-day program that provides the knowledge and tools research staff need to carry out successful community engaged research projects.

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.

The Office for the Protection of Research Subjects (OPRS) provides administrative support for the review and approval of research protocols (experiments) involving humans and human embryonic stem cells (hES).

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