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    In plain words

    AiMediQ™ in a few short answers.

    • A bedside system being developed to support the team during a Code Blue — timing, prompts, roles, and a record of the event.

    AiMediQ™ · Flagship Product

    AI-enabled support for Code Blue workflows.

    AiMediQ™ is being developed to help resuscitation teams coordinate roles, capture events, and prepare structured summaries during in-hospital cardiac arrest — supporting qualified clinicians, never replacing them.

    AiMediQ™ clinical decision-support scene during a Code Blue event with datasyteAI™ integration
    Concept visualization · deidentified
    Regulatory statusAiMediQ™ powered by datasyteAI™ is currently in the pre-market / development & validation phase.
    For institutional & healthcare-professional audiences
    Product anatomy

    Every element serves the moment of care.

    AiMediQ™ Digital Scribe interface showing live transcription, event timeline, and structured clinical documentation
    Concept visualization
    1. 01

      Ambient documentation

      Captures critical clinical words in real time, hands-free, so no detail is missed during the event.

    2. 02

      Structured event capture

      Automatically organizes timelines, interventions, medications, and rhythms into a coherent record.

    3. 03

      Clinician review

      Enables the team to quickly review, edit, and validate the note before it becomes part of the record.

    4. 04

      Secure note generation

      Generates structured, de-identified notes ready for integration with the hospital record.

    Product modules

    Four coordinated capabilities.

    AiMediQ™ Digital Scribe interface showing live speech capture, structured notes, event timeline, vitals, medications, and action items
    Concept visualization
    1. 01 · Guidance

      Guideline-aligned prompts in context.

      Contextual, protocol-aligned prompts intended to help the resuscitation team maintain situational awareness — delivered to a qualified clinician who retains full decision authority.

    2. 02 · Coordination

      One shared view of roles and timing.

      Shared role assignments, time-in-role tracking, and cue-based prompts designed to reduce coordination overhead so the team can focus on the patient.

    3. 03 · Calculation support

      Structured inputs for time-based calculations.

      Structured inputs for calculations clinicians commonly perform under pressure. Values are reviewed and confirmed by the clinician; the system does not autonomously order or administer therapy.

    4. 04 · Documentation

      The event, captured as it happens.

      Time-stamped event capture aligned with existing resuscitation record fields, designed to reduce post-event reconstruction and support quality review, debriefing, and registry reporting.

    Hardware & interface

    All visuals are labeled concept visualizations using deidentified, fictional data.

    Bedside interface — Digital Scribe concept visualization
    Bedside interface

    Concept visualization — deidentified UI, no real patient data.

    Detail crop — display
    Detail · display
    Interface — event view
    Interface · event view
    AiMediQ™ in a resuscitation bay
    Environment

    Designed for the resuscitation bay.

    Scope

    What AiMediQ™ is — and what it is not.

    Precision about intended use protects clinicians, patients, and institutions.

    What it is
    • Clinical decision support intended for use by qualified resuscitation teams
    • A structured event recorder aligned with existing resuscitation documentation
    • A coordination surface for role assignment and time-based cues
    • A platform for downstream quality review, debrief, and registry reporting
    What it is not
    • A replacement for clinician judgment, training, or ACLS certification
    • A device that autonomously administers therapy or issues clinical orders
    • A diagnostic device intended for direct-to-patient use
    • A source of medical advice for patients or the general public
    Event workflow

    Conceptual stages of a supported event.

    A high-level view of how AiMediQ™ is designed to accompany a resuscitation event. No clinical instructions, doses, or protocols are shown.

    1. session.start

      Activation

      The team activates AiMediQ™ at the start of the event; the session begins its structured timeline.

    2. roles.set

      Role assignment

      Team leader, compressions, airway, and recorder roles are captured to support coordination.

    3. event.log

      Event capture

      Actions, interventions, and observations are recorded with timestamps for the clinical record.

    4. summary.export

      Debrief handoff

      A structured session summary is prepared for review, QA, and registry workflows.

    Deployment & integration

    A credible path from conversation to evaluation.

    Institutions engage through a defined sequence that respects clinical governance, IT review, and compliance oversight — with system integrations confirmed per site.

    1. STEP 01

      Discovery

      Structured conversation with clinical, operational, IT, and compliance stakeholders.

    2. STEP 02

      Fit assessment

      Review of resuscitation workflow, documentation practice, and technical prerequisites.

    3. STEP 03

      Pilot planning

      Site-specific plan with defined success measures, safety governance, and evaluation cadence.

    4. STEP 04

      Evaluation

      Structured evaluation window with clinical, workflow, and operational endpoints.

    Institutional environment
    • Hospital identity & access

      Designed to integrate with institutional identity providers.

    • Clinical documentation

      Event data is structured for downstream integration. [CLAIM REQUIRES APPROVAL — specific EHR integrations pending validation.]

    • Registry & QA reporting

      Designed to support institutional QA and registry reporting workflows.

    Evidence & evaluation

    What we can — and cannot — say today.

    Evidence and evaluation status is published as it is approved. Nothing on this page should be read as a completed clinical validation or regulatory clearance.

    In DevelopmentOngoing

    Regulatory pathway

    Regulatory strategy — in development

    AiMediQ™ regulatory pathway is under active development. Specific submissions and jurisdictions will be disclosed once approved.

    1. PlannedIn preparation

      Clinical evaluation

      Clinical evaluation plan — planned

    2. PlannedSite selection

      Pilot program

      Institutional pilots — planned

    AiMediQ™ — institutional FAQ

    Find answers to common questions about our technology and services

    Next step

    Bring AiMediQ™ into a structured clinical conversation.

    Request a Clinical Briefing for your team, or reach out to discuss a pilot at your institution.