How do I submit a trial to be a part of the network?

  • The originating trial site will take responsibility for the following:
    • Final protocol
    • Regulatory document distribution and updates
    • Electronic database for data collection
    • Randomization, if applicable
    • Data management
    • Final data quality
    • Data analysis
  • Trials are reviewed and agreed upon by the oversite group
  • E-mail For a trial submission include the following:
    • Site PI contact information
    • Study Coordinator/Regulatory support contact information
    • Protocol
    • Data management plan
image widget
Facebook Twitter