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