Clinical Trial Management

Speed site selection with an investigator database designed to easily search, identify, and qualify sites around the world. Seamless interoperability with TI eFeasibility and eTMF.

Speed site selection with a configurable survey module to contact, assess, and prequalify sites. Screen sites for inclusion and save surveys and collected data for future use.

Accelerate site activation by simplifying the collection, completion, and finalization of critical regulatory documentation necessary for approval to bring a site online.

An investigative site file solution that reduces administration and improves speed and compliance for site personnel and study teams with digital investigative site binder processes.

A practical, secure, and compliant single access point for TMF documentation, supporting all essential document processes and reducing the time, costs, and risks of TMF management.

A shared workspace for sponsors, CROs, and sites to share and author documentation. Author and approve required documentation across the clinical lifecycle and automatically send to the LMS for training or index in the eTMF for real-time inspection readiness.