Healthcare Bundle
Healthcare bundle example
Section titled “Healthcare bundle example”This example shows how SCS bundle structure maps to a healthcare application that needs to incorporate HIPAA compliance requirements alongside internal architectural standards.
This is an advanced example — most teams start with the solo developer or team setup guides.
Bundle hierarchy
Section titled “Bundle hierarchy”bundle:prior-auth-app:DRAFT # Project bundle (AI entry point) ↓ importsbundle:acme-health-corp:1.0.0 # Domain bundle (company aggregator) ↓ importsbundle:acme-architecture:1.0.0 # Concept bundle (architecture standards)bundle:acme-security:1.0.0 # Concept bundle (security standards)bundle:acme-clinical:1.0.0 # Concept bundle (clinical workflows) ↓ importsbundle:hipaa:1.0.0 # Standards bundle (HIPAA requirements) ↓ importsbundle:meta:1.0.0 # Meta bundle (SCS foundation)When Claude Code loads the project bundle, it recursively resolves all imports and loads the combined SCD content from every bundle in the hierarchy.
Project bundle manifest
Section titled “Project bundle manifest”id: bundle:prior-auth-apptype: projectversion: "DRAFT"title: Prior Authorization Applicationdescription: AI context for the prior auth workflow application
scds: - scd:project:prior-auth-domain - scd:project:prior-auth-api-patterns
imports: - bundle:acme-health-corp:1.0.0
provenance: created_by: Engineering Lead created_at: 2025-01-15T10:00:00Z rationale: Project-specific context for prior auth developmentWhat this means for Claude Code
Section titled “What this means for Claude Code”When a developer opens Claude Code on this project, Claude loads:
- HIPAA compliance requirements
- Acme’s internal security standards
- Clinical workflow constraints
- Project-specific API patterns and conventions
All from structured, versioned files that the team reviews and maintains together.
Medical-device manufacturers: a different ontology
Section titled “Medical-device manufacturers: a different ontology”This example models a healthcare software company under HIPAA. A medical-device CDMO — a contract design & manufacturing organization building under ISO 13485, IEC 62304, and FDA 21 CFR 820 — has a different set of concepts: risk management, system architecture, verification & validation, supplier qualification, and more. SCS 0.5.0 ships a reference Domain Ontology for that market, with its regulatory concepts mapped to the standards they satisfy.