Services

The Clinical Trials Unit offers a full range of services:

• Sponsor visit coordination
• Source documentation obtention and creation
• Pre-screening, screening, recruitment, and scheduling study subjects
• Subject participation and payment reporting
• Study visit conduct and procedure coordination
• Paper or electronic case report form (CRF) completion
• Drug/device accountability and administration
• Specimen Processing, packing, and shipping
• Clinic/hospital logistics, as needed
• Data query resolution
• AE and SAE reporting