Medical software demands accuracy and regulatory oversight. The TGA classifies software as a medical device if it influences clinical decisions. IEC 62304 defines your development process requirements. Clinical data carries stricter privacy obligations than GDPR.
Most software teams discover these constraints after building something that fails regulatory review. We build compliance into the engineering process from the start. Our engineers understand clinical workflows, health data standards (HL7, FHIR), and what a TGA submission requires. The result is software that works for clinicians and satisfies regulators.
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