Agatha’s immediately available clinical solution enables Hospitals, Biotechs, Pharmaceutical companies and CROs to collect the documentation and manage the processes occurring during the course of clinical trials.


In addition to a complete set of document management functions, Agatha provides unique capabilities to greatly improve your productivity and compliance including:

  • Collaboration with external partners.
  • Management of expected documents and forms per sites / countries and per milestones (as per the TMF Reference Model)
  • Auto-classification of imported documents.
  • Auto-generation of documents and forms based on existing structured content (topics) and maps.
  • Management of pre-filled web forms for Ethic Committee and IRB review.
  • Dissemination of protocols and other corporate documents at country and site levels.
  • Management of Investigator Site File.

Contact us for a demo, or start a free trial.


Check-out the benefits that Agatha can bring to your organization: