eSP™ Software

Extensible Clinical Trial Management Software Platform

Utilizing proprietary eSP™ software, we initiate, manage, and successfully close-out your clinical trial using the shortest and most economic path. Advanced features within eSP enable quick configuration of protocol specific software. Protocol compliance is enhanced by eSP’s ability to identify protocol violations in real-time and intuitively advance investigators through protocol testing requirements.

New or updated information is automatically transmitted to and from clinical sites and our host database through eSP’s bidirectional replication processes, ensuring complete redundancy and the most timely and accurate data possible.

eSP enables:

• Remote upgrades bypassing unnecessary programming delays for protocol amendments
• Online/offline data acquisition, for added flexibility
• Comprehensive audit trail including eQuery™; full electronic data reconciliation
• Full transparency and sponsor access to patient data
• FDA 21 CFR Part 11 compliant, ensuring more consistent, reliable, and secure data

Real-time monitoring of your trial's progress is not only convenient, but allows for easily managed remote protocol changes. Electronic data clarification (eQuery) eliminates time consuming and costly paper DCFs.