Imaging that doesn't slow your science
QMENTA removes months from every stage, governing your data, running your AI, and producing audit-ready evidence across every disease area, imaging modality, and phase of work.
One governed data layer for your imaging database from training to FDA submission
Multi-site research studies coordinated and harmonized from day one
From first scan to legal-grade evidence, without rebuilding
In production across 250+ imaging sites worldwide
The right product for every imaging program
Whether you're running a Phase III trial, building an AI model, or quantifying brain injury for a legal case, there's a QMENTA product built for that workflow.
Trials
Governed neuroimaging for industry-regulated clinical studies.
—Real-time QC, AI, and central review in one system
—GxP and 21 CFR Part 11-ready for FDA and EMA
—Sponsors, CROs, and core labs in one platform
Explore Trials →
Foundation
Collect, organize, develop, and deploy imaging AI across any disease area.
—Research, Study, and Clinical tiers in one system
—Neuro, cardiac, oncology, and beyond
—AI firms, academic centers, and hospitals welcome
Explore Foundation →
Legal
Automated DTI quantification for TBI litigation.
—Automated segmentation of 33 fiber tracts
—Trusted by imaging centers and law firms nationwide
—Pay-per-scan. No commitment, no specialist needed
Explore Legal →
From research to clinical practice in five years. Against an industry norm of a decade or more.
CAVS-MS connected 10 leading academic institutions, processed hundreds of patients' imaging data through a single validated pipeline, and produced the evidence that contributed to the revision of the McDonald Criteria, all on QMENTA.