Clinical Intelligence Platform

More ReliableClinical TrialEndpoints.

Neuriora unifies clinician training, participant screening, digital assessment, real-time intelligence, and source-documentation QA to improve the quality, consistency, and reliability of clinician-rated trials.

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Neuriora

Controlled Training

Move raters through narrated courses, VR simulation, mastery gates, and certification flows that produce measurable reliability.

Clinician completing a narrated psychiatric rating course

Deterministic Scoring

Enforce anchor-based, evidence-linked scoring support so clinical teams can defend decisions without surrendering clinician control.

Clinical interview transcript linked to psychiatric scoring anchors

Protocol Execution

Programmatically execute psychiatric inclusion and exclusion logic with ScreenWise instead of relying on fragmented manual interpretation.

Participant profile connected to protocol eligibility criteria

Clinical Intelligence Solutions

One Platform. Five Clinical Intelligence Solutions.

Everything needed to improve the quality, consistency, and reliability of clinician-rated clinical trials.

SimLab AI-patient training interview workspace

SimLab

AI-Powered Clinician Training & Certification

Standardize rater performance using realistic AI patient simulations, adaptive training, certification, and remediation.

ScreenWise patient profile and protocol eligibility review

ScreenWise

Intelligent Participant Screening

Evaluate protocol eligibility with deterministic, evidence-linked screening that improves enrollment quality and consistency.

Neuriora Assess dashboard on tablet and phone

Neuriora Assess

Digital Clinical Assessments

Conduct clinician-rated assessments in an intuitive workflow designed for protocol compliance and high-quality source data.

NSI live clinical interview quality monitoring

NSI

Real-Time Clinical Intelligence

Monitor interviews as they happen with AI-powered protocol adherence, evidence sufficiency, scoring support, and quality insights.

DocuGuard source-document quality review workspace

DocuGuard

Source Documentation QA

Review clinical documentation for completeness, consistency, ALCOA+ principles, and audit readiness before data submission.

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Integrated Platform

Built as one integrated clinical intelligence platform, not isolated point solutions.

Neo connects protocol constraints, scale-aware reasoning, structured evidence, and human review context across SimLab, ScreenWise, Neuriora Assess, NSI, and DocuGuard.

Protocol logicScale-aware reasoningStructured evidenceHuman oversight

Built for the Study Team

Designed for Every Clinical Trial Stakeholder

One platform delivers role-specific value across the organizations and clinicians responsible for endpoint quality.

Clinical development sponsor executive

Sponsors

Improve endpoint quality across global studies.

Clinical research organization program leader

CROs

Standardize assessments across investigators and sites.

Clinical research site investigator

Clinical Research Sites

Reduce operational burden while improving protocol adherence.

Central rater conducting a remote assessment

Central Raters

Receive intelligent guidance while maintaining clinical judgment.

Clinical operations leader monitoring study quality

Clinical Operations

Monitor quality, consistency, and study performance in real time.

Platform Overview

See Neuriora in Action

Operating Principles

What remains constant across every MVP.

The product changes with the workflow. The controls underneath it do not.

Protocol aligned

Training, interview execution, and decision logic begin with the study protocol and the instrument being used.

Study protocol and instrument workspace

Human governed

AI supports preparation, evidence review, and quality control while clinical responsibility remains with qualified people.

AI support checks alongside a clinician decision

Evidence linked

Scores, feedback, and protocol decisions stay connected to the interview or source information that supports them.

Interview transcript linked to a MADRS score

Role controlled

Raters, trainers, administrators, and validators work through distinct access paths with clear responsibilities.

Role selection for raters, trainers, administrators, and validators

Connected Evidence

Every MVP contributes to the same study record.

The stack moves from readiness to eligibility, visit execution, scoring quality, and source review without losing the evidence produced at each stage.

01

SimLab

AI-Powered Clinician Training & Certification

Workflow stage

Readiness

Connected output

Training, simulation, benchmark, and certification record

02

ScreenWise

Intelligent Participant Screening

Workflow stage

Eligibility

Connected output

Criteria-level outcome with linked evidence

03

Neuriora Assess

Digital Clinical Assessments

Workflow stage

Study visit

Connected output

Structured response-to-score record and live audit trail

04

NSI

Real-Time Clinical Intelligence

Workflow stage

Scoring quality

Connected output

Probe, evidence, and consistency signal

05

DocuGuard

Source Documentation QA

Workflow stage

Source QA

Connected output

ALCOA+ review and issue-resolution record