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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 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).

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 Trial Innovation Network (TIN) is a collaborative national network that focuses on operational innovation, excellence and collaboration and will leverage the expertise and resources of the CTSA Program.

Learn more about the Trial Innovation Network

Contact UIC's TIN Liaisons 

 

Certain types of clinical trials are required by law to be registered when they begin, and the information updated throughout the study.

FDA regulations and guidance documents are accessible from this site as well as international GCP guidance documents on which FDA has collaborated and that have been adopted as official FDA guidance.

From study design to participant recruitment and engagement, the Trial Innovation Network continues to add self-service tools and resources to help investigators throughout the entire life cycle of their projects.

Access the TIN Clinical Trial Toolkits

The OPRS website and ResearchMatch- a national clinical trial registry- offer a directory of research studies at UIC that are actively enrolling subjects.

The Office of Research and Development (ORD) aspires to discover knowledge, develop VA researchers and health care leaders, and create innovations that advance health care for our veterans and the nation.

The CCTS collaborated with members of the Office of the OVCR Quality Improvement Program to develop a set of standard case report forms. The forms should be useful for any investigator initiated clinical trials and can be customized to an individual study.

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