The CTSI supports a range of services that facilitate translational research at UF:
Statistical consulting, programming, data management and data entry services for clinical and translational studies.
A large-scale “database” integrating information from UF’s clinical and research environments.
Consultation, auditing, SOP development, batch releases and training to ensure Good Clinical Practice (GCP)/ Good Manufacturing Practice (GMP)/ Good Lab Practice (GLP).
Secure, Web-based application designed to support traditional case report form data capture for research studies (provided at no cost for use with any research project).
Guidance and assistance for IND, IDE and FDA application, regulatory and compliance requirements.
Expert consultation on ethical issues in the design and conduct of biomedical research.