CPR Pharma 2016
  • Project specific, primary contacts at CPR
  • Regular Sponsor update meetings or teleconferences on study status
  • Protocol development
  • Local sponsorship
  • Site contracting and budget negotiations
  • Ethics submissions and regulatory correspondence
  • Comprehensive study start-up-activities

Monitoring

  • Site Initiation Visits and reporting
  • Interim study monitoring visits and reporting
  • Remote monitoring activities
  • Trial Master File maintenance
  • Site budge oversight and invoicing activities
  • Study Close-out
  • Safety reporting 
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