Annuo Health Cloud

Think it, Build it, Run it.

Helping healthcare teams design, build, and deploy safe, compliant-by-design AI medical device software & digital-health applications — fast.

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Network of clinicians connected across the Annuo Health Cloud

What we do

We believe in person-centred care. We focus on getting health teams access to compliance-ready building blocks to design, build, and run regulated health-AI software — faster.

Faster innovation

Spin up governed health software and deploy CI/CD in minutes — not months — with risk controls pre-wired.

Built-in governance

Comprehensive medical device software lifecycle management aligned to ISO standards.

Healthcare-first

FHIR-aware patterns, PHI identification management, and regional data-residency controls.

How it works

1Define your use case

Describe the users, condition, patient demographics, and your goals. Annuo Health Cloud matches your profile + workspace plan.

2Generate your workspace

The platform provisions the resources, repositories, pipelines, docs, and automated flows — all pre-configured.

3Launch with confidence

Export evidence packs for audits and certification, SBOM, and metrics. Move from prototype to pilot with traceability intact.

Clinician holding app

Who we help

Health-AI Startups

Accelerate launches and reduce regulatory overhead.

Clinics & Hospitals

Deploy secure tools and assistants that integrate with existing systems.

Researchers & Innovators

Prototype responsibly and publish results with full governance traceability.

Annuo Health Cloud global coverage map

Global reach

Supporting healthcare innovation across continents with secure regional hosting, interoperability by default, and governance frameworks aligned to local regulations.

🇬🇧 United Kingdom 🇪🇺 European Union 🇺🇸 United States 🇦🇺 Australia

📜 Compliance & Observability

Built for regulated healthcare across major markets:

  • supports audit-ready logging and monitoring, SBOM-based software transparency, and privacy-by-design controls (including PHI de-identification where appropriate).

  • Aligns with IMDRF regulatory frameworks and standards - the UK MDR 2002 (MHRA), EU MDR/IVDR (Regulation (EU) 2017/745 & 017/746),and Canada (SOR/98-282), FDA (21 CFR 820 / QMSR) and Australia (Therapeutic Goods MDR 2002).

  • supporting standards such as ISO/IEC 27001 and IEC 62304 for secure, traceable software lifecycle controls.

  • Audit logging and Privacy impact assessment (DPIA)

    • 🔗 Data & Standards

    Interoperability and terminology are implemented using recognized healthcare standards (FHIR, HL7, DICOMweb, SNOMED CT, LOINC) to support traceable, auditable clinical data exchange—aligned with quality, risk, and AI governance expectations (FDA QMS, ISO 13485/14971, ISO/IEC 42001).

    🛂 Identity & Access

    Standards-based SSO and access control (SMART on FHIR, OAuth2/OIDC, Microsoft Entra ID) with RBAC for least-privilege access, auditability, and regulated clinical workflows.

    🧩 Integrations

    Integrates with Microsoft 365 services and standards-based clinical interfaces, including event-driven FHIR subscriptions where supported, to enable controlled data exchange, traceability, and operational audit readiness in regulated healthcare workflows.

    Need another region or connector? We extend via Azure subscriptions with unified RBAC and logging.