Study Start-Up Checklist For Digital Clinical Trials
Source: Florence Healthcare
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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