The Office of Research Regulatory Affairs (ORRA) Monitoring Unit is responsible for monitoring all UAMS-sponsored investigator initiated clinical research trials conducted under an IND or IDE. If your research study requires an IND or IDE, this group will work with you to ensure your study is monitored as required by federal regulations (21 CFR 312.56 and 21 CFR 812.40 ).
- Suzanne Carlisle, Monitoring Specialist, 501-686-7976
- Shawna Owens, Monitoring Specialist, 501-603-1206
- Laura Adkins, Monitoring Specialist, 501-686-6092