Technology Built for Clinical Reality

Yes. HIPAA, HITECH breach notification, the minimum necessary rule, protected health information handling, consent, audit trails, and data residency are designed into the build from the start. Clixlogix works under a signed Business Associate Agreement wherever the engagement touches PHI, and every release is prepared to hold up to a security review.

Clixlogix builds integration across major EHR and EMR systems using HL7 v2, FHIR R4, and SMART on FHIR, with CCDA document exchange and DICOM for imaging. Integration is scoped to your specific workflow so the record moves cleanly across the systems you already run.

Yes. Clixlogix builds de-identified data pipelines to the Safe Harbor and Expert Determination methods, handles behavioral health data under 42 CFR Part 2, and supports IRB aligned consent capture and electronic case report forms for clinical research.

Clixlogix builds to the traceability, validation, and documentation that a Software as a Medical Device pathway expects, aligned to IEC 62304 and ISO 13485, and structured to support an FDA 510(k) or De Novo submission led by your regulatory team.

Protected health information is encrypted at rest and in transit, access is scoped by role with full audit logging, and data residency follows your regulatory requirements. Security controls are chosen at architecture time, not added before launch.

Yes. Recent healthcare work includes an AI medical imaging platform that measures spinal Cobb angle from radiographs, a cardiac care application, and a public health data platform. The case studies below carry the full engagement narrative and the outcomes the buyer signed against.