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Site Management

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Services for Sponsor/CRO

Clinical Research Coordinator

  • Project Feasibility Study
  • Site Information Collection
  • Site Fast Start-up
  • Subject Recruitment (Local Site)
  • Subject Management
  • Data Management
  • Sample Management
  • Study Supply and File Management
  • Internal Audit
  • Sponsor Audit, Site Self-inspection, CFDA Inspection Coordination
  • Project Management

Subject Recruitment

  • Phase I to Phase IV
  • Healthy Subject & Non-healthy Subject
  • Local Site & External Resource
  • Online & Offline

Call Center

  • TC Follow-up
  • Post-marketing Safety Monitoring
  • Online Customer Service
  • Coordination/Dispatching Center
  • Drugs Pre-sales/After-sales Consultation
  • Message Delivery Platform
  • Tele-survey

 

Services for Study Sites/Investigator

Clinical Trial Management

  • Professional CRC Allocation
  • Study File Management
  • Subject Recruitment and Management
  • Study Supply Management
  • Data Management
  • EC and GCP Office Communication
  • Safety Information Management

Study Site Management

  • Study Site SOP Establish and Update
  • Study Site Information Management Platform Set-up
  • Tutor of Regulatory Approval and Filing
  • Training for Investigator and other site staff
  • Site Self-inspection
  • Budget Negotiation and Management
  • Study Site Business Development and Promotion

Project Experience

*As of Q1 2020

SMO clinical trials

Hospitals

Cities