Technology that advances care.

Yes. We design and build patient-data systems to HIPAA requirements, with encryption, access controls and full audit trails built into the architecture. We also align with HL7 and FHIR standards for clinical data exchange where relevant. Compliance is an engineering requirement from the first design decision, not a review at the end.

Yes. We build HL7/FHIR integrations that connect new platforms to existing EHRs, lab systems and connected medical devices, unifying data that otherwise sits in separate silos. Integration scope is mapped during discovery so it fits your current clinical workflows.

Patient data is encrypted in transit and at rest, access is controlled and logged at a granular level, and every system carries a full audit trail. We design for HIPAA's technical safeguards throughout the build rather than adding security as a final step.

Most healthcare engagements run as a dedicated squad, engineering, QA and a delivery lead, working in two-week sprints with a demo at the end of each. Staff augmentation is also common when a provider or pharma team wants to extend in-house capacity instead.

A focused patient portal or telehealth feature typically ships in 10 to 14 weeks given the added compliance review, while a full clinical platform runs 5 to 9 months. We size the real timeline during discovery once we understand your regulatory and integration requirements.

Every engagement is scoped and quoted individually, accounting for compliance requirements, integrations and the size of the platform. After a short discovery call, you get a clear, itemised estimate within 48 hours.