The CTSI Service Center provides a range of services and resources to investigators performing translational research across campus.The CTSI Service Center’s programs, resources and core facilities can assist you in:
Initial consultations for all services are offered at no cost. If a study requires special or extended involvement of staff, cost may be assessed. We will discuss all available options at the first consultation.
Please contact any of the CTSI services listed below as early in the process as possible, even before you have submitted a grant proposal.
Need to print this information to distribute at an event? Download up-to-date, printable PDFs of CTSI Research Services and other programs here.
Not sure where to start? Research navigators can help direct your team to the right resources. Please see the cards below for a list of CTSI services and contacts.
Design a Study
Design a study, determine appropriate sample size and perform statistical analysis.
Assistance with engaging citizen scientists in research projects.
Tabs for resources, training, IRB, safety and ethics, standards and templates and professional associations.
The RDDC helps investigators refine objectives into testable hypotheses, choose study designs, develop data analysis plans, and perform power analyses and sample size calculations.
The core provides researchers with tools and resources designed to help conduct systematic reviews for a wide variety of subjects.
The Health Science Center Libraries (HSCL) at the University of Florida offer specialized expertise in searching and critical appraisal of the literature to researchers developing clinical and translational studies.
Data Management and Software
Research Data Management, Algorithms, Research Software Design, Implementation and Support
Capture data with this secure, web-based application.
Receive guidance on IND, IDE application and reporting requirements.
Consultation, auditing, SOP development, batch releases and training to ensure GCP, GLP and GMP.
Receive guidance on regulatory submissions, informed consent, IRB submissions and ClinicalTrials.gov registration and compliance.
Consult an expert on clinical trials and Data Safety Monitoring Boards.
Assistance with developing recruitment strategies, creating recruitment materials and evaluating recruitment methods.
Recruit participants from the community, including underrepresented populations.
Access clinical data for cohort identification and recruiting, and to answer research questions.
Implement grant-funded research in real-world settings throughout the state.
Addresses critical roadblocks in clinical research and accelerates the translation of novel interventions into life-saving therapies.
Explore and validate feasibility for clinical studies across the NCATS Clinical and Translational Science Award (CTSA) consortium.
Facilities for outpatient and inpatient research including nursing, dietary and lab support.
Clinical research study monitoring services.
CAP-accredited facility specializing in biological sample procurement and storage.
Consult with experts on applying human-validated assessment measures of behavioral concomitants of disease or therapeutic interventions.
Use structural and functional MRI services for human subject research.
Simulate processes to promote patient safety.
Receive training and services for induced Pluripotent Stem Cell (iPSC) derivation and related reprogramming technologies.
Use metabolomics services, including mass spectrometry, nuclear magnetic resonance and bioinformatics.
Design and perform genetics and pharmacogenetics studies with expert consultation.
Receive assistance in moving your compound from the lab toward clinical trials.