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The Regulatory Support and Advocacy Core provides centralized, accessible regulatory support, advice and guidance.

The OVCR Quality Improvement Program hosts a toolbox of standard tracking forms that helps investigators capture essential information in an organized fashion.

The CCTS Research Navigator helps UIC clinical and translational research investigators and study coordinators find the information and resources needed to navigate research ideas through the university system. The Research Navigator will guide you through a complex research landscape to place you on the right path to the right resources at the right time.

ResearchMatch has a simple goal – to bring together two groups of people who are looking for one another: (1) people who are trying to find research studies, and (2) researchers who are looking for people to participate in their 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).

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.

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

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