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Prototype demoCareStrand is being demonstrated with synthetic data. Production deployment is coming soon.What the demo includes
Prototype demo · production platform coming soon

One patient.Every system. Connected.

CareStrand is the clinical context, workflow and application-governance layer that helps clinicians work across fragmented records and approved tools—without replacing the systems that remain authoritative.

Synthetic data onlySource systems stay authoritativeHuman-controlled actionsInternational by design

The public website and workspace show a product prototype. Production connectors, formal assurance and live clinical deployment are not yet available.

CareStrand prototype

CareStrand synthetic connected clinical workspace

EPRHospital record
AIApproved applications
GPPrimary & community
Demonstration available now
Connects rather than replacesEPRs, diagnostics, imaging, documents and shared records remain authoritative.
Standards-ready architectureDesigned around FHIR, HL7, DICOM, MESH, APIs and context launch.
AI with boundariesApplications receive task-specific context and explicit permission tiers.
Built to travelA global core with configurable jurisdiction, organisation and pathway packs.
The problem

Clinical work is fragmented even when records are digital.

A single appointment may require repeated searches across order communications, imaging, letters, theatre records, primary care, community systems and new clinical applications.

01

Context is repeatedly rebuilt

Clinicians search for the same patient in multiple systems and manually reconstruct what matters for the current task.

02

Actions become disconnected

Results, referrals, letters and follow-up promises can sit in different queues with unclear ownership and completion.

03

Every new tool can add a silo

AI, monitoring and specialist applications often need separate integrations and governance for every organisation and record system.

The CareStrand layer

Connect. Understand. Act.

CareStrand turns a fragmented environment into one coherent clinical workflow while preserving source provenance and human control.

Explore the platform

01

Connect

Bring together approved information and launch routes across hospital, primary, community, patient and specialist systems.

  • FHIR, HL7 and document exchange
  • DICOM and imaging context
  • SSO and patient-context launch
02

Understand

Compile the minimum relevant context for the clinician, task and approved application—with citations back to source.

  • Patient and encounter briefing
  • Ask the whole record
  • Conflicts, amendments and missing evidence
03

Act

Draft, review, approve and track work across systems without giving AI or browser automation unrestricted authority.

  • Open-loop task tracking
  • Human approval and receipts
  • Governed write-back when supported
Three core capabilities

An intelligence and workflow layer—not another record viewer.

Clinical Context Compiler

The right information for the right task

Patient, encounter, role, purpose, application, sensitivity and provenance are combined to create a minimum-necessary context package.

See how context is compiled

Open-Loop Guardian

Track promises until they are complete

CareStrand extracts and confirms actions, assigns ownership, watches connected systems for evidence and escalates unresolved work.

Explore open-loop safety

AI Application Gateway

One governed route for approved tools

Ambient documentation, evidence assistants, diagnostic AI, monitoring, pathway and patient tools receive only the permissions they are approved to use.

Explore the application gateway

See the product

A calm workspace around the patient and the work.

The clinician interface keeps identity, source evidence, open actions and context controls visible. Technical integration detail is progressively disclosed only when it is needed.

  • Today’s clinic and preparation state
  • Longitudinal timeline, results and documents
  • Connected source launchers with provenance
  • Ask the Record with citations and uncertainty
  • Actions followed until the loop is closed
CareStrand guided synthetic clinic demonstration

Current synthetic prototypeDesktop, tablet and mobile
Safe by design

Confidentiality, provenance and human control are part of the product.

CareStrand is designed to limit context before an AI or connected application receives it, keep source systems authoritative, and retain evidence of every governed action.

Review the safety model

Minimum necessary

Context is assembled according to role, purpose, task and approved application—not copied indiscriminately.

Source linked

Every clinical statement can retain its source, version, status, freshness and amendment history.

Human controlled

Clinical content and actions remain drafts or suggestions until an appropriately authorised person reviews them.

Auditable

Access, context, application, model, approval and write-back evidence can be retained as structured receipts.

Diagram showing where CareStrand sits between systems of record and clinical applications

Where CareStrand sitsIt complements records rather than replacing them
International by design

One reusable core, configured locally.

CareStrand separates the global product from local identity, terminology, privacy, integration and pathway requirements.

CareStrand Core

ContextWorkflowApp governanceAudit

Jurisdiction & organisation

IdentifiersTerminologyPrivacyConnected systems

Specialty & pathway

ClinicReferralFollow-upLocal policy
Help shape CareStrand

We are looking for healthcare and technology partners.

Speak to us about a synthetic demonstration, a bounded non-production integration, a clinical workflow pilot, or connecting an approved application through the CareStrand gateway.

CareStrand Insights

Read the thinking behind the product.

Clinical workflow, interoperability, source trust and governed AI—written for teams trying to make fragmented healthcare systems work as one.

View all insights

CareStrand is currently a synthetic prototype for demonstration and product development. It is not connected to production clinical systems and must not be used with identifiable patient information or for clinical decision-making.

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