SureAdhere for Clinical Trials
Protocol compliance is essential to achieving successful clinical study outcomes. SureAdhere supports clinical trial sponsors, contract research organizations (CROs), and trial sites to quickly identify and engage participants who need support, improve protocol compliance, and prevent loss-to-follow-up.
Identify Protocol Deviations Quickly
Comprehensive and real-time compliance data (e.g., amount of investigational product (IP) dispensed, ingested, or applied) allows for daily adherence intervention when required
Engage Directly with Participants
Configurable dose reminders & detailed dosing histories support complex treatment regimens. Secure SMS messaging and virtual visits enable secure participant engagement when required
Virtual Visits Available in Spring 2024.
Ask us about using it.
Integrate External Systems
Interoperability with MEMs solutions and other participant companion applications make comprehensive data aggregation seamless. Direct integration of clinical data sets with external trial systems (i.e., IRT, EDC, CDR) enables seamless clinical workflows and decentralized trials.
Safe and Secure
SureAdhere complies with US HIPAA and European GDPR data privacy regulations. The platform is 21 CFR-Part 11 compliant and is regularly audited by trial sponsors and CRO’s. Our global support team provides comprehensive service level agreements based on local time zones.
Our Partner in Clinical Trials
Connect With Us
Connect with our team for a demo or learn more about our platform