Clinical Development Liaison

In Order To Keep You Connected, We Will:
  • Translate your clinical dosing regimen into drug supply requirements
    • Quantity and Strength

  • Create packaging options and label designs

  • Manage your label approval process
    • Develop English master label
    • Collate country-specific translations
    • Manage proof generation and review
    • Routing for final approval

  • Develop a global distribution strategy and written plan
    • Includes cold chain methodology

  • Forecast your drug supply requirements
    • For study initiation through last subject/last visit

  • Monitor your progress against clinical development milestones

  • Conduct IVRS specification development and reviews
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