Putting patients first:

Alethium Consent streamlines site operations.

Consent requirements often burden sites, diverting their attention from patient care to operational management. Alethium Consent alleviates this strain by tackling all complex, tedious, difficult, and high-risk tasks, thereby enhancing value beyond traditional site-based management.

Consent signature screen

Consent Anywhere

Seamlessly manage patient consent via paper, eConsent, or hybrid modes, accessible across all devices and locations.

Consent with Certainty

Alethium eliminates the risk of incomplete ICFs, ensuring all signers have consented to the correct type, language, and version.

Improved Patient Understanding

Maximize content comprehension by utilizing hyperlinks and other interactive features to enrich understanding, reduce site burden and remain compliant.
Consent Report showing a line chart

Screening Efficiently

Screen participants with advanced Inclusion/exclusion criteria to guarantee eligibility, ensuring precision and accuracy in selection.

Deviation Protection

Count on our intelligent tools to detect and prevent deviations related to consent, providing reliable support for your site.

Real-Time Data

Ensure trial health with actionable notifications and real-time analytics, keeping you informed and proactive every step of the way.

eSource

Reduce site burden, stream data capture, eliminate transcription errors, get real-time reporting and remote monitoring, and align your trial with FDA and EMA recommendations.

Audit Log at the Core

Alethium’s event-driven architecture ensures the audit log remains the source of truth for your clinical trial.

How can we help with your study?

The Alethium eClinical Platform removes the time, cost, and risk from large, complex, multinational clinical trials. Tell us about your needs and a member of our team will connect with you soon.