- Conduct Close-out Visit and Prepare Report
- Perform Final On-Site Drug Accountability
- Return or Dispose of Unused Drug Supplies
- Return or Dispose of Unused Non-Drug Supplies
- Verify CRF's and Source Documents on File at Site
- Verify Shipment of All Laboratory Specimens
- Review Regulatory Documents for Completeness
- Review Record Retention Policy
- Send Follow-up Letter to Investigators
Services: Site Closeout
