Clireo eCTD




Features Overview

Clireo eCTD provides a validated all-in-one cloud solution for pharmaceutical and biotechnology companies to manage all of their global regulatory activity. Coupled with the Clireo eDMS and Clireo Templates, Clireo eCTD creates a complete platform that includes submission planning, document authoring / review / approval, and comprehensive eCTD publishing capabilities.

How it works

Clireo eCTD is a cost-effective, cloud-based global eSubmission solution. Clireo eCTD is the only solution that is not limited by users allowing you to easily add publishers regardless where in the world they are working.

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Clireo eCTD assembles and publishes globally compliant eCTD submissions with drag and drop ease from the eDMS, eMPM, or eTMF solution.

Clireo eCTD also integrates a toolbox of critical PDF management capabilities. Our patent pending HTML 5 based link management system allows users to create and edit PDF hyperlinks directly in the browser without having to download and edit documents on the desktop.

Clireo eCTD is supported by industry first such as Microsoft Azure infrastructure, always up-to-date publishing, and a rules engine that supports ease of upgrade for regulatory standards and validation.

All-in-all, Clireo eCTD is the industry’s fastest, most convenient and cost effective submission management solution.