Neuratrial
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    Governed clinical trial orchestration

    Clinical trial execution, orchestrated.

    Neuratrial connects authorised sources so study teams can identify risk, assign ownership and retain evidence.

    Systems of record stay authoritative. Neuratrial coordinates work between them.

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    NVIDIA Inception Program member

    Member of NVIDIA Inception Program. Built for sponsors and CROs.

    Orchestration flow

    Source signal to accountable closure

    Governed loop

    Neuratrial

    Governed orchestration

    Representative sources

    CTMS

    EDC/CDMS

    eTMF

    QMS/Safety

    Docs & comms

    Other sources

    APIs and exports

    Detect

    Explain

    Route

    Track

    The execution gap

    Your systems hold the record. The trial still runs between them.

    A milestone, query, document, decision and follow-up can each sit in a different place. Neuratrial turns those signals into governed action with ownership and evidence.

    Signal

    Risks, queries, blockers and changes that need review.

    Context

    The source evidence and study impact behind the signal.

    Action

    The next step, owner, due date and escalation path.

    Closure

    The decision, outcome and evidence retained for inspection.

    How orchestration is governed

    Configure the operating model before scaling it.

    The orchestration layer is mapped to each customer's systems, roles, approval points and evidence expectations.

    Step 1

    Define sources

    Agree which systems, files, exports and workspaces are authorised for the workflow.

    Step 2

    Set review logic

    Configure thresholds, rules, AI scope and human review points for the study team.

    Step 3

    Assign accountability

    Route work to the right role with due dates, approvals and escalation paths.

    Step 4

    Retain the record

    Preserve the source evidence, rationale, decision and outcome for later review.

    Configure once for a workflow, then reuse the pattern across studies.

    Existing systems

    Representative sources, not a fixed integration list.

    Neuratrial is system-neutral by design. It can map to authorised systems, documents, exports, APIs and approved workspaces while preserving validated systems as records of authority.

    CTMS and study milestones
    EDC/CDMS and clinical data
    eTMF and document repositories
    QMS, safety and quality systems
    Finance, resource and vendor data
    Approved APIs, exports, trackers and communications

    Workflows

    One orchestration layer. Start with the workflow that matters most.

    Start with a high-friction workflow, validate it with users and representative data, then expand the same model across studies and functions.

    Risks, actions, dependencies

    Study execution and issue management

    Coordinate milestones, site signals, monitoring findings, vendor dependencies and open actions.

    Activation blockers and owners

    Study start-up and site activation

    Track prerequisites, submissions, approvals, essential documents and activation blockers.

    Completeness and quality

    TMF and inspection readiness

    Support completeness, quality checks, reconciliation and remediation while eTMF remains authoritative.

    Queries and decisions

    Data and lock readiness

    Connect unresolved queries, documents, decisions and vendor deliverables that affect lock readiness.

    The same pattern can extend to enrollment, monitoring, quality, vendor management, resource planning and protocol-amendment impact.

    Governance

    AI supports the workflow. People remain accountable.

    Clinical operations require repeatability, evidence and accountable decisions. Neuratrial uses controlled logic where consistency is required and governed AI where language and context add value.

    Designed to support risk-proportionate oversight, timely escalation, clear responsibilities and traceable records in GCP-regulated clinical operations.

    Controlled logic

    Rules, thresholds, calculations, mappings and deterministic decisions remain version-controlled where repeatability is required.

    Governed AI

    AI can assist with unstructured content interpretation, classification, summarisation, contextualisation and prioritisation within a defined and reviewable scope.

    Human accountability

    Qualified users retain control of consequential actions and all clinical, medical, safety, quality and regulatory decisions.

    Governance assurances shown where factually supported

    Source-linked outputs and decision history
    Role-based access and data isolation
    Versioned rules, prompts and models
    Human approval at defined decision points
    Customer data is not used to train models
    Deployment and data boundaries aligned to agreed security and data-residency requirements
    Approved model selection rather than dependence on one model provider

    Organisational clinical memory

    Make every study easier to run than the last.

    Capture decisions, owners, evidence and outcomes as work happens, so teams can understand precedent without reconstructing context from email, meetings and trackers.

    Adoption model

    Prove value in one workflow. Scale on the same layer.

    Select a representative workflow, map the real systems and decisions, configure governance, validate with users and measure the operational result before scaling.

    1

    Select

    Choose a priority workflow with clear operational friction, ownership and measurable outcomes.

    2

    Connect

    Map the real systems, documents, decisions, dependencies and evidence used by the study team.

    3

    Configure and validate

    Configure the rules, AI scope, roles, approvals and escalation paths, then validate them with representative data and users.

    4

    Scale

    Extend the proven orchestration pattern to additional studies, functions and portfolio workflows.

    Company

    Built for the realities of clinical trial execution.

    Neuratrial is a Singapore-headquartered clinical technology company helping sponsors and CROs coordinate complex trial workflows without replacing systems they already trust.

    Read about the company

    Headquarters

    Singapore

    Audience

    Sponsors and CROs

    Operating model

    Governed workflow orchestration

    Boundary

    Systems of record stay authoritative

    FAQ

    Questions clinical leaders usually ask first

    Does Neuratrial replace our CTMS, EDC or eTMF?

    No. Neuratrial works above authorised systems and preserves them as the authoritative records. It adds cross-system context, action coordination and evidence of follow-through.

    Can we begin with one workflow?

    Yes. Neuratrial is designed for phased adoption around a representative, high-value workflow, followed by expansion on the same governed orchestration layer.

    Does the AI make decisions autonomously?

    No. Scope, rules, review points and escalation paths are configured. Qualified users retain responsibility for clinical, medical, safety, quality and regulatory decisions.

    Where can Neuratrial be deployed?

    Deployment and data boundaries are agreed with each customer. Depending on the selected architecture, the platform can support dedicated Neuratrial-managed or customer-controlled environments.

    Is customer data used to train models?

    No. Neuratrial does not train models on customer data.

    Next step

    Where does coordination break down in your trial?

    Bring one workflow that repeatedly loses time, context or ownership. We will map how Neuratrial can connect the existing process and govern the path to closure.

    Discuss a priority workflowSend workflow context

    Neuratrial

    Clinical trial orchestration for sponsors and CROs.

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