PharmaTrail offers the Lucie platform, a private‑blockchain‑based suite for clinical trial data management that provides immutable audit trails and secure, regulatory‑compliant storage. The solution includes Study Manager, eConsent, ePRO/eCOA, and EDC modules with drag‑and‑drop design, real‑time mobile capture, and API integration, helping sponsors and CROs streamline study setup, execution, and regulatory submission.
Funding
$4.1M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Clinical trial sponsors and CROs struggle with fragmented, insecure data capture systems that lack immutable audit trails, making regulatory review slow and increasing risk of data manipulation or loss.
Solution
PharmaTrail’s Lucie platform provides an end‑to‑end clinical trial solution built on a private blockchain layer that guarantees tamper‑proof audit trails for all study data. The suite includes Study Manager, eConsent, ePRO/eCOA, and EDC modules, each designed for intuitive use by sites, investigators, and participants. Integrated drag‑and‑drop form building, automated scheduling, and real‑time mobile data capture streamline study setup and execution, while blockchain‑anchored records ensure compliance with GDPR, HIPAA, 21 CFR Part 11 and other regulations. The platform also offers secure archival, version‑controlled amendments, and API connectivity for real‑world evidence device integration, enabling faster regulatory submissions and smoother stakeholder trust.
Target Audience
Primary customers are pharmaceutical sponsors and contract research organizations that run multi‑site clinical trials and require compliant, secure data management solutions.
Features
- Private blockchain ledger providing immutable audit trails and secure data locking for all trial data
- Drag‑and‑drop Study Manager with flexible event scheduling, amendment tracking, and role‑based team management
- Integrated eConsent app with multimedia education, remote video communication, and configurable electronic/wet‑ink signatures
- ePRO/eCOA mobile application for participant‑entered outcome capture and clinician‑entered eClinRO entry
- User‑friendly EDC with source data verification, query management, and comprehensive audit trail visualization
- Seamless data flow between modules and API readiness for real‑world evidence device integration
- Blockchain archival service for long‑term, tamper‑proof storage and compliant data export