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Remedy AI
Remedy AI

We turn complexity into clarity.

We build AI tools for healthcare — from medical documentation to clinical trial recruitment. Data stays in Europe, built to EU law, with clinicians always in command.

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01 — The problem

Medicine is drowning in paperwork.

European healthcare doesn't lack knowledge or commitment. It suffers from an excess of everything that stands between clinician and patient: forms, systems, codes, evenings spent at a keyboard.

20.9%
of physicians spend 8+ hours a week in the EHR outside working hours — unchanged since 2022AMA, 2025
1.2M
doctors, nurses and midwives missing across the European UnionEuropean Parliament / OECD, 2024–25
80%
of clinical trials fail to meet their patient-enrollment targets on timeJMIR (meta-analysis) / Tufts CSDD, 2020–24
68%
of oncology patients were never offered a clinical trial — yet 84% of those asked say yesCross-sectional study, 2024

The problem isn't doctors. It's everything standing between them and the patient — and that can be redesigned.

Outlook

The shift is already underway.

$187.7B
projected global AI-in-healthcare market by 2030 — growing 38.5% a yearGrand View Research, 2025
51.9% → 38.8%
the drop in clinician burnout after 30 days with an ambient AI scribeJAMA Network Open, 2025
2.5M
AI-drafted visit notes in one year at a single health system — 16,000 documentation hours returned to physiciansNEJM Catalyst / Kaiser Permanente, 2025

AI should augment, not replace — human autonomy is the first principle of the WHO guidance on AI in health. That is exactly how we build.WHO guidance, 2021 / 2024

02 — The ecosystem

One ecosystem. One foundation.

Every product is a different front of the same fight — from the practice room, through hospital systems, to clinical research and the mental health of medical teams. All of them stand on one foundation: data in the EU, pseudonymization by design, humans making the decisions. The ecosystem keeps growing — and every new product inherits that foundation on day one.

Remedy Core

  • Data in the EU
  • Pseudonymization by design
  • Humans decide

Clinical core

The signal originates in practice, not in a sprint.

Every medical and health-adjacent application at Remedy is built with the substantive support of a team of psychiatrists and psychologists — from designing the visit flow to validating every AI suggestion. We don’t just "write medical apps". We braid technology with clinical judgement.

psychiatrists · clinical psychologists · AI engineers

One signal. Separate strands.

03 — Products

Many fronts. One fight.

EVA

Electronic Visit Assistant

The practising physician's digital toolkit

Leave the room with the notes done.

Remedius EVA

EVA

Electronic Visit Assistant

The practising physician's digital toolkit

Leave the room with the notes done.

EVA listens to the visit, keeps drug knowledge at hand and drafts the documents — the physician reviews, corrects and signs.

  • AI Scribe

    Turns the patient conversation into structured documentation in real time — for your sign-off, never instead of it.

  • Drug Atlas

    A full pharmacopedia with interaction checking — before the prescription reaches the patient, not after.

  • Remedius Report

    Discharge summaries and certificates drafted from the treatment history in minutes, not evenings.

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IDEA

Intelligent Documentation & Electronic Administration

A practice EHR powered natively by AI

An EHR built on FHIR, not on habit.

Remedius IDEA

IDEA

Intelligent Documentation & Electronic Administration

A practice EHR powered natively by AI

An EHR built on FHIR, not on habit.

A natively FHIR R4-compliant health record with an ICD-10 assistant and clinical decision support — psychiatry today, primary care next.

  • Native FHIR R4

    Interoperability as the default, not the roadmap — EHDS-ready from day one.

  • ICD-10 assistant

    Suggests the right codes as you write — no more digging through classifications.

  • Clinical decision support

    Contextual guidance for psychiatry — with the clinician always holding the final word.

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Inclusia

Clinical-trial pre-screening

Clinical-trial pre-screening

Evidence from the source, not a verdict.

Inclusia

Inclusia

Clinical-trial pre-screening

Clinical-trial pre-screening

Evidence from the source, not a verdict.

Inclusia reads medical records and maps them against trial protocol criteria — many protocols in parallel, in minutes rather than hours. OCR runs entirely in the browser, records never leave the site, and the investigator always makes the call.

  • Source citations

    Every criterion comes with the exact record excerpt — dated, page-referenced, ready to verify.

  • Pharmacotherapy reconstruction

    Automatic treatment history: doses, switches, wash-out periods and prohibited medications.

  • Multi-protocol & verification queries

    One record analysed against many trials at once — and where data is missing, Inclusia drafts the questions to ask.

Inclusia supports the work of clinical researchers — it is not intended for diagnosis or clinical risk assessment. Results require verification by qualified medical personnel.

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After Duty

Mental wellness for first responders

Wellbeing for uniformed services

Support that never reads over your shoulder.

After Duty

After Duty

Mental wellness for first responders

Wellbeing for uniformed services

Support that never reads over your shoulder.

A mental-health platform for police officers, firefighters, paramedics and soldiers — encrypted journaling, AI reflection and clinical oversight, with zero access to content for superiors.

  • E2E-encrypted journaling

    Entries no superior — and not even we — can read.

  • AI reflection

    Gentle, daily insight into mood and patterns — support, not judgment.

  • Clinical oversight

    Clinicians behind the platform; HIPAA-ready architecture on a SOC 2 path.

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04 — Compliance

Regulation is our starting line.

Europe has just written the world's strictest rules for medical AI — the AI Act and EHDS, with hard deadlines through 2029. Most of the market will retrofit. We were designed inside them.

  • GDPR by design

    RODO/GDPR

    Data minimisation and lawful bases built into the architecture, not the terms of service.

  • EU data residency

    EU

    Processed and stored exclusively in the European Union — no exceptions, no asterisks.

  • PII pseudonymization

    PII-0

    Personal data is pseudonymized before it ever reaches a model — in Inclusia, still on the device.

  • FHIR R4

    FHIR R4

    The interoperability EHDS demands is in our DNA — not on our roadmap.

  • Human-in-the-loop

    HITL

    No clinical decision happens without a human: AI drafts, the clinician decides.

  • EU AI Act

    AI ACT

    Engineered to high-risk system requirements today — ahead of the 2027–2028 deadlines that will define this market.

05 — Who it's for

Different perspectives. A shared interest.

For clinicians

We build tools that give you time back — not another system to serve. Test us, challenge us, co-create: the final word is always yours.

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For institutions & regulators

Full compliance documentation, auditability, and data that never leaves the EU. We're a partner for pilots, deployments and hard questions — the hard questions are our favourite part.

Security & compliance →

For investors

European medical AI just got its rulebook and its calendar. Teams compliant from day one won't be paying for this moment — they'll be paid by it.

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Remedy AI

Complexity has an expiry date.

Let's talk about your institution, your trial, or your portfolio.