Study Start-Up Checklist For Digital Clinical Trials

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Study start-up can be one of the most time-consuming and challenging parts of a clinical trial. Technology should make this process faster, but too often, it makes the process more complicated instead. 

Five Florence employees with clinical research backgrounds came together to craft a checklist designed to walk sites through the process of tech-enabled study start-up.  

This checklist will help you quickly and compliantly:

  • Coordinate with your sponsor and IRB
  • Integrate multiple systems, like eISF, CTMS, and eConsent platforms
  • Organize and track regulatory documents
  • Communicate with PIs and collect eSignatures

You can also reuse this checklist for every new study to make all of your digital trials more efficient.

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