How it works
Built for performance, large volumes of data, and globally dispersed users, Clireo eDMS scales from the smallest biotech to the largest global Pharmaceutical, Biotech, or Medical Device company.
Clireo eDMS provides all of the rich features required by the industry with the simplicity of the cloud and compliance of a qualified platform and CFR 21 Part 11.
Completely configurable and flexible, Clireo eDMS allows users to meet their requirements while maintaining integrity and compliance. Clireo eDMS includes workflow, library services, electronic and digital signatures, and bulk document handling capabilities. Competing systems require multiple vendors and software programming to achieve similar capabilities as Clireo eDMS.
Integration is also a core capability of Clireo eDMS, this includes synchronization of Documents from FTP, SharePoint, and sign-on with your active directory. Additionally, Clireo eDMS is tightly integrated with Clireo eCTD, giving you end-to-end document creation, management, rendition, submission, and tracking capabilities.
Clireo allows users to import Microsoft Project plans to populate the project schedule and document hierarchy. Clireo also provides support for the document structure and metadata models of the DIA EDM Reference Model.