- Conduct Monitoring Visit and Prepare Report
- Collect Completed CRF's
- Perform on Site Drug Accountability
- Assess Subject Compliance with Dosing
- Resolve Data Clarifications with Investigators
- Verify CRF's Appropriately Record SAE's
- Verify SAE's are Reported to IRB
- Review and Update Regulatory Files as Needed
- Maintain Training of Site Personnel
Services: Interim Monitoring Visits
