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