Centrally track clinical trial site document creation at start-up

Sponsors can centrally track documents at site startup

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The Florence eBinder SuiteTM is a HIPAA and 21 CFR Part 11 compliant tool designed to make virtual document access easy for sponsors without burdening the sites.

  • Keep compliant and secure: our system is CFR 21 pt 11 and HIPAA verified before delivery
  • Create a trial master file (eTMF) and manage trial site queries between CRAs and coordinators
  • Track progress toward request completion
  • Access documents remotely for regulatory doc review or source data verification (SDV) by your CRAs