HIPAA compliant architecture
PHI encryption, BAAs with all vendors, audit trails, role-based access. Built compliant from commit zero, not retrofitted.
HIPAA compliant, EHR-integrated, patient-centered. We build healthtech that scales from clinic to system without compromising security.
Security and patient outcomes, designed from day one.
PHI encryption, BAAs with all vendors, audit trails, role-based access. Built compliant from commit zero, not retrofitted.
Epic, Cerner, Athena, custom EHRs via FHIR APIs. We speak HL7 fluently. Real integration, not screen-scraping.
Accessibility (WCAG 2.1 AA), mobile-first design, plain language. Healthcare UX has unique requirements; we get it.
Video, async messaging, secure file sharing. We integrate Twilio, Doxy.me, or custom WebRTC solutions.
LOINC, SNOMED CT, RxNorm integration. We model clinical data correctly so analytics and AI actually work.
We generate the artifacts your auditor needs: risk assessments, security policies, pen test reports, BAA templates.
Digital health — patient engagement platform
Orbital Health needed to scale patient onboarding from hundreds to hundreds of thousands without breaking the bank or the compliance posture. Their existing monolithic EHR integration couldn't keep up.
Built a patient engagement platform on AWS with FHIR-based EHR integration, async messaging, real-time notifications, and HIPAA-compliant analytics.
HIPAA-eligible services and clinical-grade infrastructure.
We build on HIPAA-eligible infrastructure (AWS BAA, GCP healthcare). Our code follows HIPAA Security Rule requirements. We sign BAAs as needed and work with your compliance officer for risk assessments.
Yes — Epic, Cerner, Athena, Allscripts, MEDITECH, and custom EHRs. We use FHIR R4 (modern) and HL7 v2 (legacy) as appropriate. We can build custom adapters when needed.
PHI encrypted at rest (AES-256) and in transit (TLS 1.3), strict role-based access, comprehensive audit logging, automated threat detection, regular penetration testing. We follow the principle of least privilege throughout.
For software-as-a-medical-device (SaMD) products, we work with your regulatory affairs team. We can help with technical documentation for 510(k) submissions, but you'll need regulatory counsel for the actual filing strategy.
Granular consent management, easy-to-understand consent flows, audit trails of every consent decision, support for state-specific requirements (CCPA, state health privacy laws). Patients can revoke consent and we honor it across all systems.
We work with your clinical team to define success metrics, build measurement into the product, and support pilot studies. We don't run clinical trials ourselves — that requires IRB and clinical research expertise.
Book a confidential intro call. We'll discuss HIPAA, EHR integration, and your specific clinical workflow.