555x450_projectmgmt

CLINICAL TRIAL PROJECT MANAGEMENT:

  • Study and Protocol Design and Development
  • Consent Forms Preparation
  • Monitoring Plans
  • Preparation of IRB Submissions
  • Study Site Contract and Budget Development
  • Development of study specific site investigator qualification criteria
  • Pre-study site-investigator qualification
  • Site Initiation Visits Customized for Your Study:
    • Comprehensive Protocol Training
    • Comprehensive Device Training
    • Training to Promote Protocol Compliance
  • Interim Monitoring
    • Customized monitoring plans
    • Data and site monitoring according to monitoring plan only by device trained monitor
    • Efficient practices
  • Site Close-out Visits
  • Final Reports

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