Clinical Study Coordination
We have a long history of coordinating clinical trials. Our experienced staff excels at patient recruitment and has a proven track record of patient retention in long term studies. Each of our team members has GCP (good clinical practice) guidelines training and certification.
Services Include:
- IRB (institutional review board) approvals
- Regulatory document management
- Patient recruitment
- Patient consent
- Source document completion
- CRF (case report form) completion both paper and online
- Study drug handling
- IVRS (interactive voice response system) randomization and drug management
- Adverse Event and Serious Adverse Event reporting
- Blood collection and handling
- -20 C freezer storage with backup generator
- Staff dangerous goods certified for dry ice shipments
- Data query resolution
- Record storage
