eSP Software
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electronic Short Path software platform Utilizing proprietary eSP™ software, nSpire Health initiates, manages, and successfully closes your clinical trial using the shortest and most economic path. Advanced features within eSP enable quick configuration of protocol specific software. Compliance is enhanced by eSP’s ability to identify violations in real-time intuitively advancing investigators through protocol testing requirements. eSP. Features and Benefits • Remote upgrades bypass unnecessary programming delays for protocol amendment • Online/offline data acquisition provides additional flexibility • Comprehensive audit trail including eQuery, full electronic data reconciliation • Full transparency and sponsor access to patient data • FDA 21 CFR Part 11 compliance ensures more consistent, reliable, and secure data The Right Choice – For your Clinical Trial Quick protocol configuration and enhanced study compliance, through eSP software’s clinical protocol predicted events and testing requirements, shorten deployment time. Investigator sites can download subject data directly to eSP software, eliminating data errors associated with manual entry and improving principle investigator site productivity, minimizing time to data lock. Proven in millions of subject tests worldwide, eSP using the KoKo Spirometer is the number one choice for research spirometry in the clinical trial industry, delivering the most accurate test results possible. The eSP spirometry module guides site technicians to perform quality spirometry and bronchial challenge maneuvers. eSP controls the home-based component of clinical trials, utilizing the PiKoLogic® electronic diary / lung health monitor to instantly and securely transfer data to nSpire Health’s central server for quality review, data management, and sponsor access. eSP’s architecture has been continually reinvented and expanded to include the most advanced and sophisticated protocol and electronic data management capabilities. eSP’s complete transparency improves respiratory trial productivity. The Right Choice – For Subject Compliance Protocol driven workflow through eSP software controls and guides the testing process. Real-time continuous monitoring of protocol compliance improves data inclusion rates and eliminates unnecessary patient efforts. New or updated information is automatically transmitted between clinical sites and our host database through eSP’s bidirectional replication processes, ensuring the most timely and accurate data possible. Inspiring Respiratory Health

The Right Choice – For Data Confidence eSP provides real-time feedback to site technicians, and study subjects (eDiary) on issues regarding testing quality and protocol compliance. Reporting modules supprt timely feedback to investigators, monitors, and sponsor project team members. The eSP platform and nSpire Health’s clinical trial data management processes are Part 11 compliant, providing data redundancy and backups, as well as sample tracking of your data through a secured closed-system architecture. eSP offers maximum flexibility for protocols and protocol amendments while promising a...