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.
Auditing and Monitoring
Within the Clinical Research Office Compliance Group, auditing and monitoring are conducted by the Clinical Trials Auditing Team (CTAT).
Contacts
For information related to the CRO Compliance Group, please contact the audit team at CRO-Compliance@ufl.edu.
Compliance Leadership
Ashley D Anderson MBA, ACRP-CP
Staff
Misty Hinson BA, ACRP-CP
Megan Roberts MS, CCRC
Victoria Sylva CCRC, ACRP-CP
Terrena Smart MPH, CCRC
Education or training needs? Visit the Office of People and Culture.
