The CTSI Service Center provides a range of services that help research teams navigate the UF research landscape and the regulatory and compliance environment:
Get personalized answers to your questions about conducting research at the UF Academic Health Center.
CTSI experts can help with IRB submissions, Research Administration and Compliance reviews and ClinicalTrials.gov requirements.
Guidance and assistance for IND, IDE and FDA application, regulatory and compliance requirements.
Consultation, auditing, SOP development, batch releases and training to ensure Good Clinical Practice (GCP)/ Good Manufacturing Practice (GMP)/ Good Lab Practice (GLP).
Expert consultation on ethical issues in the design and conduct of biomedical research.
Resource for study participants as well as investigators and study staff in the responsible conduct of clinical trials
The CTSI connects investigators at UF and other institutions to several resources available to support and participate in multisite studies, including the Trial Innovation Network’s SMART IRB, and the OneFlorida Clinical Research Consortium.