The Alethium
eClinical Platform
A value-driven solution for complex global trials.
Alethium’s full suite of services easily translates your study protocol into a customized platform so you can focus on outcomes.
The Alethium eClinical Platform is automated to scale across multiple locations and languages without incurring extra costs or schedule disruptions.
Unlock the Full Potential of Global Studies
The Alethium eClinical Platform was created to automate multi-source study data collection for optimal accuracy, efficiency, and readability, empowering clinical teams to monitor critical outcomes in real-time, reducing study risk.
Enhanced Compliance
Communication with participants is critical to ensure compliance, prevent withdrawal, and ensure optimal data collection. Alethium’s system enables email, SMS, phone, and video calls with the touch of a button all while keeping an audit trail of every touch point and ensuring PII remains secure.
Alethium delivers nuanced notifications for higher participant engagement, while alerting the clinical team on the real-time status of all compliance, data entry, technical, or safety updates.
Simplify your Most Complex Studies
Real-time scalability with complex integrations for large, multinational studies is the hallmark of Alethium’s eClinical Trial Platform.
From intelligent consent management, interactive longitudinal reports, hassle-free EDC/IRT and medical device integrations, effortless televisits and more, Alethium ensures participants are compliant, investigators are informed, and data is secure.
Unlimited Scalability
Designed to deliver verifiably accurate data with infinite scalability, Alethium’s eClinical Trial Platform easily meets the most data-intensive trial needs.
Whether running large-scale long-duration Phase 3 studies with tens of millions of data points, or large reports scheduled for anytime-availability, the Alethium system scales in step with your operational needs.
Record Time to Market
Infinite Integrations
Alethium’s event-based infrastructure seamlessly integrates medical devices, IRTs, EDCs, EMRs, CTMS, and IxRS for efficient and accurate data collection and analysis.
With advanced ID verification, dual enrollment prevention, participant payment, participant transportation, and central lab integrations, Alethium’s next-generation platform ensures the highest level of data integrity and safety for the most complex decentralized trials.
Core Features
Consent Management
Flexible consent with intelligent ID Verification manages the most complex consent scenarios including vulnerable populations, pediatrics and guardianship.
Advanced Screening
Our modular screening tools let investigators quickly identify and convert qualified candidates into active study participants.
Interactive Longitudinal Reports
From user behaviors, interactive data flagging, and data thresholds, Alethium’s interactive longitudinal reports keep investigators, CRAs, and Sponsors on the pulse of every study.
Secure
The Alethium Platform is ISO 27001, HIPAA, GDPR audited and compliant. All PHI is encrypted by default.
Secure
The Alethium Platform is ISO 27001, HIPAA, GDPR audited, and compliant. All PHI is encrypted by default.
Scalability
Designed for long-term global studies, Alethium manages exponential study growth with ease, regardless of country or location.
Notifications
Our highly-configurable notification system delivers timely alerts to the right users through various channels including email, SMS, TEAMS, and Slack.
Telehealth
Secure, robust and seamless, Alethium connects doctors and participants with ease and convenience, regardless of location.
eCOAs
Built to reduce licensed eCOAs setup time by half, Alethium exceeds the rigorous standards of the industry’s leading eCOA copyright providers.
Notifications
Our highly-configurable notification system delivers timely alerts to the right users through various channels including email and SMS.
Televisits
Secure, robust and seamless, Alethium connects investigators and participants with ease and convenience, regardless of location.
eCOAs
Built to reduce licensed eCOAs setup time by half, Alethium exceeds the rigorous standards of the industry’s leading eCOA copyright providers.
Participant Compliance
Reporting
Alethium delivers a host of features to give investigators, Sponsors, and CRAs an ongoing and complete view of participants current and historical compliance records.
Alerts
Alethium’s nuanced alerts handle the most complex requirements with ease to bring participants back to compliance quickly.
Quick-Contact
Real-time multi-channel communication helps investigators return participants to compliance quickly.
Advanced Features
Defining the Future of Clinical Studies
Study and Business Integrations
Alethium effortlessly integrates with medical devices, IRT, EDC, EMR, TMF, CTMS, and more.
Flexible Architecture
Every study on Alethium is isolated by design, running in its own secure cloud instances with dedicated resources for greater control, customization, and security.
Custom Interface
Powerful tools along with custom web and responsive mobile interfaces. Alethium delivers purpose built apps for Participants, CRAs and Sponsors.