Browse All Resources

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).

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.

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.

Pages