Clinical Trial Progress Monitoring Report Form
Trial Title
Protocol Number
Sponsor
Site Name/Location
Principal Investigator
Date of Visit
Type of Visit
Initiation
Interim
Close-Out
Summary of Activities Performed
Subject Enrollment Status
Investigational Product Accountability
Informed Consent Documentation
Protocol Deviations/Violations
Adverse Events/Safety Issues
Data Quality (CRFs, Source Documentation)
Action Items/Recommendations
Monitor Name
Monitor Signature
Date