Intuitive eCRF Form Builder
Build clinical data capture forms around your protocol with a visual, no-code workflow.
All-in-One Research Platform
Stop jumping between spreadsheets and fragmented software. From eCRF and EDC to eTMF, manage complex clinical research data in one connected workspace.
Platform Features
Integrated tools designed to streamline clinical research workflows without splitting study data and documents across disconnected systems.
Build clinical data capture forms around your protocol with a visual, no-code workflow.
Define edit checks, identify discrepancies, and support a consistent query-resolution workflow.
Manage enrolled subjects and filter, search, and explore the clinical data your team needs.
Organize Trial Master File (TMF) and Investigator Site File (ISF) records alongside the study workspace.
Track study progress and inspect key metrics through project-level statistics and dashboards.
Export study data and use role- and project-scoped workflows designed for multi-site research operations.
Pricing Plans
Choose a starting point for a pilot, an academic study, a multi-site registry, or an enterprise research program.
Start a small study and evaluate the core workflow.
Core collaboration and data management for one study team.
Advanced quality management for organizations running multiple studies.
Custom operations, scale, and support for institutions.
Published prices describe the current product catalog. Taxes, payment availability, limits, and enterprise terms may vary; confirm final terms before purchase.
Frequently Asked Questions
Clear answers for research teams evaluating an integrated clinical data workspace.
Figgle is a web-based clinical research workspace that brings eCRF design, electronic data capture, data review, analytics, and study document organization into one application.
Figgle supports individual investigators, academic research teams, hospitals, multi-site registries, and CRO workflows through project membership and role-based access.
Yes. A project can combine form-based clinical data workflows with study document and electronic lab notebook tools, reducing the need to switch between separate systems.
The application uses authenticated sessions, project-scoped permissions, and role-based actions. Study teams should still validate their protocol, regulatory, and institutional requirements before production use.
Contact Us
Tell us about your study and the services you need. We will review your request and reply using the email address you provide.
Email us
goldenegg@figgle.itWebsite
figgle.itRegister cases using published study forms and manage data within each project.
Explore data alongside published variable definitions and review validation results.
Randomization is optional and follows study configuration and execution permissions.
Manage study documents and case data in a shared project context.
Account subscriptions and study team membership are separate management scopes.
Research data access is managed through authentication, project roles, institution scope and change history.