Data doesn’t fix itself, we build it right from the start.
Our platforms are purpose-built for integrity and traceability, ensuring quality and compliance by design.
Our proprietary data model guarantees structured, standardized, and interoperable data from day one. It aligns with clinical vocabularies, enforces consistency, and makes data instantly actionable for research, care, and analytics.
We recover, standardize, and transform legacy or fragmented data — from spreadsheets to outdated systems — into structured, compliant, and research-ready formats. By bridging the gap between obsolete tools and modern platforms, we reclaim untapped data utility.
From scripted bots to advanced AI-powered assistants that understand context, learn over time, and support complex user needs in healthcare, education, and events.
Designed specially for rare conditions, the platform supports structured data capture, longitudinal tracking, and data-driven insight generation.
Electronic Case Report Form system — designed to capture structured clinical trial data efficiently and in compliance with regulatory standards.
A scalable registry designed for real-world data and clinical trials, enabling standardized oncology data collection and analysis.
Electronic Patient-Reported Outcomes platform — enabling real-time symptom reporting and outcome tracking directly from patients.
An automated system for adverse event tracking, attack reporting, signal detection, real-time alerts, and seamless regulatory compliance.
Secure, real-time patient diary designed for remote trials and continuous monitoring in chronic care contexts.
From clinical notes to integrated DICOM, it surpasses EMR/HIS platforms, wnforces consistency, enables research readiness, and supports AI integration.