Goldway Medical Technology
Medical software engineering

Software that earns clinical trust.

Goldway designs and builds medical software for care teams in Canada and Vietnam — remote monitoring, clinic operations, diagnostics and analytics — with privacy, interoperability and usability engineered in from the first sprint.

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Every showcase application runs on synthetic data.

Standards we design around
  • HL7® FHIR® R4
  • HL7 v2
  • DICOM
  • SMART on FHIR
  • LOINC
  • WCAG 2.2 AA
  • OWASP ASVS
Showcase

Six applications. One engineering standard.

Interactive concept applications that show how we approach real clinical workflows. Open any of them — every screen runs on synthetic data, right in your browser.

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Capabilities

From clinical insight to production software.

One accountable team across research, design, engineering, integration and operations.

Clinical workflow discovery

Shadowing, interviews and journey mapping with clinicians, nurses and administrators to find the problem worth solving.

Product design

Interfaces designed for interruption, fatigue and glanceability — tested against WCAG 2.2 AA from the first prototype.

Software engineering

Web, mobile and cloud applications with typed code, automated tests and reproducible builds.

Interoperability

HL7 v2, FHIR R4 and DICOM integration, terminology mapping and interface engines that connect to existing HIS, LIS and PACS.

Responsible AI

Assistive AI with human-in-the-loop review, source grounding, evaluation sets and clear limits on what a model may decide.

Security & operations

Threat modelling, least-privilege access, audit trails, monitoring and incident runbooks for systems that must stay up.

Capabilities
How we work

A delivery process built for regulated environments.

  1. 01

    Discover

    Clinical context, users, risks and success measures — documented and agreed before code.

  2. 02

    Design

    Prototypes tested with real users, a risk register and an architecture that fits your environment.

  3. 03

    Build & verify

    Short increments with automated tests, traceable requirements and security review at every release.

  4. 04

    Launch & operate

    Staged rollout, monitoring, support and continuous improvement backed by evidence.

Our approach

Safety is a process, not a badge.

We do not lead with certificates. We lead with practices you can inspect: threat models, traceable requirements, test evidence and human oversight wherever software meets a clinical decision.

Read our engineering approach

Privacy by design

Collect the minimum, separate identities from clinical data and make retention explicit.

Security engineering

Threat models, OWASP ASVS controls, dependency hygiene and independent testing.

Traceability

Every requirement links to design, code and test evidence — ready for audits and regulated pathways.

Human oversight

Software supports clinical judgement; it never silently replaces it.

Canada · Vietnam

Two markets. One standard of care.

We design for the language, privacy rules and care settings of each market — not a translated afterthought.

CA

Canada

Interfaces ready for bilingual delivery, privacy design that considers PIPEDA and provincial health-information laws, and integration with HL7 and FHIR ecosystems.

VN

Vietnam

Vietnamese-first interfaces, privacy design aligned with the Law on Personal Data Protection, and integration with hospital HIS, LIS and PACS environments.

Insights

Thinking ahead.

Perspectives on medical technology, digital health and safety updates from public regulators.

Our journal is taking shape. Explore the showcase in the meantime.

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Contact

Let’s build what care teams need next.

Tell us about your workflow, your users and your constraints. We will suggest the smallest useful next step.

Request a demoShowcase