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    PathFree Technologies
    Current page: Evidence

    In plain words

    Our evidence work in a few short answers.

    • No. It is investigational and not cleared for clinical use. Every item on this page is labeled with its real status.

    Evidence & clinical evaluation

    Evidence, labeled honestly.

    PathFree develops AiMediQ™ and datasyteAI™ through a staged evidence plan: technical validation, structured simulation, institutional pilots, and — where appropriate — peer-reviewed clinical evaluation. This page is the source of truth. Nothing here is presented as more mature than it is.

    Evidence library

    Filter by category and status.

    Filters
    Planned StudyPlanned

    AiMediQ™ regulatory strategy and clinical evaluation plan

    Date
    [APPROVED DATE]
    Authors / Institution
    PathFree Technologies
    Population / Setting
    In-hospital cardiac arrest, adult inpatient (planned)
    Endpoint
    Structured description of intended use, risk analysis, and evaluation objectives supporting regulatory submission.
    Result summary
    [CLAIM REQUIRES APPROVAL] — publicly reportable outputs will be listed once the regulatory strategy is finalized and approved for disclosure.
    Limitations
    This is a planned regulatory and evaluation workstream. No clinical outcomes, effectiveness, or safety claims are made at this time.
    No approved claim IDs yet
    No public source yet
    Clinical StudyPlanned

    AiMediQ™ clinical evaluation plan (institutional pilots)

    Date
    [APPROVED DATE]
    Authors / Institution
    [APPROVED PARTNER INSTITUTIONS]
    Population / Setting
    In-hospital cardiac arrest, adult inpatient — specific units to be defined per site.
    Endpoint
    Workflow, coordination, and documentation endpoints agreed with each institution as part of the pilot plan.
    Result summary
    Not yet reported
    Limitations
    No enrollment has occurred. This entry describes a planned evaluation, not an in-progress or completed study.
    No approved claim IDs yet
    No public source yet
    SimulationPlanned

    In-simulation workflow evaluation (design phase)

    Date
    [APPROVED DATE]
    Authors / Institution
    [APPROVED SIMULATION PARTNER]
    Population / Setting
    High-fidelity resuscitation simulation with qualified clinical teams.
    Endpoint
    Coordination, documentation completeness, and post-event summary quality relative to current practice.
    Result summary
    Not yet reported
    Limitations
    Simulation results, when available, will not be presented as clinical efficacy in real patient care.
    No approved claim IDs yet
    No public source yet
    Technical ValidationIn Progress

    Internal technical validation — platform behavior and change control

    Date
    Not yet reported
    Authors / Institution
    PathFree Technologies
    Population / Setting
    Not yet reported
    Endpoint
    Deterministic behavior of orchestration, versioning of prompts and protocols, and change-control conformance.
    Result summary
    Not yet reported
    Limitations
    Technical validation covers platform behavior. It does not, on its own, constitute clinical validation.
    No approved claim IDs yet
    No public source yet
    How to read our evidence

    Not every data point is the same kind of data point.

    We distinguish clearly between planned work, pilot observations, simulation results, and peer-reviewed clinical evidence. Please read status labels before drawing conclusions.

    Planned work

    A defined intent — protocol, plan, or partnership — that has not yet generated data. Planned work does not demonstrate effectiveness or safety.

    Simulation results

    Observations from controlled, high-fidelity simulation with qualified teams. Informative for workflow and coordination; not equivalent to clinical outcomes in real care.

    Pilot observations

    Structured, site-specific observations under an approved pilot plan. Useful for feasibility, adoption, and workflow signals; not, on their own, a controlled clinical trial.

    Peer-reviewed clinical evidence

    Results that have completed formal peer review and publication. Where a claim requires this level of evidence, we will not make the claim until it exists.

    What we do not do
    We do not infer clinical efficacy from a patent, press release, prototype, investor presentation, testimonial, or pilot announcement. We do not convert planned milestones into completed studies.
    Bibliography

    References cited across the site.

    External references we draw on in design and communication. Placeholder entries reflect items pending confirmation by the internal claims register.

    1. 01
      [APPROVED CITATION] — American Heart Association resuscitation guidance referenced in AiMediQ™ design work.
      Placeholder pending claims-register confirmation of the exact citation and edition.
    2. 02
      [APPROVED CITATION] — ILCOR consensus on science with treatment recommendations, referenced in protocol configuration design.
      Placeholder pending claims-register confirmation.
    Bibliography is maintained alongside the claims register.
    Research collaboration

    Build the clinical evidence base with us.

    We work with institutional research partners on structured evaluation, simulation studies, and pilot programs. Reach out to explore a collaboration.

    Propose a Research CollaborationDiscuss a Pilot