Research Navigation and Regulatory Assistance


The CTSI Service Center provides a range of services that help research teams navigate the UF research landscape and the regulatory and compliance environment:

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).

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.