Within the Clinical Research Office Compliance Group, auditing and monitoring are conducted by the Clinical Trials Auditing Team (CTAT) along with education and training needs developed by the Education and Training Specialist.
The Clinical Trials Auditing Team (CTAT) provides ongoing auditing for complex through low risk clinical trials. Audits are conducted per the outlined review frequency in the DSMP. Routine, random, and “Off Cycle” audits may also be conducted for any cancer-relevant externally-sponsored studies. All auditing activities are performed consistent with ICH GCP guidelines. The CTAT audit process is also intended to evaluate the effectiveness of current training, education and monitoring practices. Findings may translate to modifications in Standard Operating Procedures (SOPs), policies or ROS activities. For information regarding this process please reference the Clinical Trials Audit Manual.
The Clinical Research Office (CRO) Compliance Office provides initial and ongoing education and training opportunities for UFHCC CRO Staff and investigators.
Within the Clinical Research Office Compliance Group, auditing and monitoring are conducted by the Clinical Trials Auditing Team (CTAT)
On line form to request an audit
For information related to the CRO Compliance Group, please contact the audit team at CRO-Compliance@ufl.edu.