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

The Partners.org virtual Regulatory Binder assists research sites in achieving and maintaining regulatory compliance and ensuring the highest standards of human subject research.

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

The purpose of the NIH Clinical Research Toolbox is to provide a Web-based information repository for investigators and staff involved in clinical research.

Investigators who need to translate a research protocol into lay language for informed consent documents and/or IRB submission may benefit from the University of Michigan’s "Simplification Guide to Medical Terms."

ClinicalTrials.gov is a registry and results database of publicly and privately supported clinical studies of human participants conducted around the world. Investigators can learn more about national clinical studies, including relevant history, policies, and laws.

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.

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