INDUSTRIES / HEALTHCARE
Care data, governed
We help healthcare organizations connect clinical systems with consent and access rules enforced by design.
Clinical data is spread across systems that were never designed to share, and every connection carries consent, access and retention obligations. Clinicians need the record without friction, and the same record must not be broadly readable. Those rules belong in the architecture, not in policy and hope.
How we help
Patient platforms and clinical integration
Patient-facing services and the integration layer beneath them, built against interoperability standards rather than bespoke file exchanges.
- HL7 and FHIR-based interface design
- Patient identity and record matching
- Consent scope carried through every interface
Security architecture for PHI
Access models, encryption and logging designed around protected health information, so least privilege and full auditability are properties of the platform.
- Role and purpose-based access to PHI
- Read-level audit logging, not only writes
- Break-glass access with mandatory review
Clinical data platforms
Data platforms where consent scope, retention class and access rules travel with the record, so analytics and reporting inherit the same constraints as the source system.
- Consent and retention modeled as first-class data
- De-identification pipelines for secondary use
- Lineage from reported figure back to source
Applied AI under clinical governance
Document extraction, operational forecasting and triage support, scoped so a clinician remains the decision-maker and every model input and output is attributable. We do not use client data to train or fine-tune models, unless a client asks us to in writing for their own dedicated model.
- Data minimization before any model sees a record
- Model documentation, versioning and monitoring
- Clear separation from clinical decision-making
Standards your organization is held to
We do not hold these certifications on your behalf. Our work is to design controls against these standards and produce the evidence your organization needs to demonstrate them.
Health-data rules we design for
US: HIPAA Privacy and Security Rules. UK: NHS Data Security and Protection Toolkit (DSPT). UK and EU: GDPR and UK GDPR special-category health data. UAE: Department of Health Abu Dhabi and Dubai Health Authority health-data rules. These are the rules healthcare organizations answer to. We are not certified or approved under any of them; we design the controls and evidence that help your organization meet them.
Health-data safeguards
These regimes all expect technical safeguards for health information. We architect and document those controls (access, audit, integrity and transmission security) so your organization can evidence them. The compliance posture remains yours.
Consent management
Consent has scope, duration and a withdrawal path. We model it as enforceable state that every read and every downstream pipeline checks, rather than as a flag captured once at registration.
Retention schedules
Record-retention obligations vary by record type and jurisdiction. We encode those schedules into storage and archival design so retention and disposal are executed and evidenced by the platform.
Least-privilege access to PHI
Access should be granted by role and by purpose, scoped to the care relationship, and reviewed. We design the authorization model and the review mechanics that make that workable at clinical speed.
Auditability of every access
In health data, reading a record is itself an event worth recording. We build audit logging that captures reads as well as writes, retains them appropriately, and makes them queryable when a question is asked.