Enhance Your Clinical Trial Operations & Site Engagement

Provide generic, clinical systems, and study-specific training in a single clinical e-Learning Management System

Support both role-based and task-based training in your studies

Utilize any format to deliver precise training, including documents, PPTs, videos, SCORM, and xAPI

Manage site staff responsibilities, designate study tasks to qualified site staff, and automatically assign training based on delegation

Transfer training credits across trials for site staff to eliminate repetition

Immediately transfer auto-generated training certificates to your eTMF

Automatically distribute country-specific packages

Seamlessly track milestone-based progress and regulatory approval

Customize & send site feasibility questionnaires

View data visualization dashboards on study startup progress & metrics with multiple drill down layers

Track patient recruitment and improve retention in a single tool

Screen patients and schedule visits in an intuitive interface

View real-time patient recruitment enrollment heatmaps

Provide patient recruitment and retention resources to sites

Utilize performance metrics - including prescreen data, patients enrolled, withdrawal, and screening failures - to make proactive decisions

Enable a single point of entry for all trial resources with single sign-on, including one-click access to EDC, IxRS, Central Labs, and more

Provide study-specific workspaces to enable collaboration with sites and the socialization of scientific knowledge through Q&A or KoL forums

Distribute global or country-specific newsletters and multimedia content

Seamlessly communicate with context-specific local and global study contacts via messaging and video conferencing options

Automate study document distribution to new sites

Receive document submissions from site staff with front-end QC and an automated integration to send them directly to your eTMF

Utilize a real-time electronic Investigator Site File (eISF) accessible by sites at any time

Easily export the complete trial document package, including audit trails and critical reports for sites, at the study’s end with one click

Centralize your distribution of Investigator Brochures, SUSAR, & Periodic SUSAR brochures on a global scale

Enable investigators to electronically acknowledge distributions

Automate distributions to new trials and new sites

Automatically transfer IBs and SUSAR acknowledgments to your eTMF

Empower CRA’s and local affiliates to remotely monitor safety reports