| name | ceap-quality-governance |
| description | Use for CEAP quality engineering, automated test generation, security checks, compliance validation, policy gates, auditability, and regulated enterprise or MedTech engineering review. |
CEAP Quality Governance
Use this skill when a request needs quality, security, compliance, or regulated-delivery controls.
Workflow
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Classify the change risk.
- Determine whether the change touches security, privacy, regulated workflows, data integrity, APIs, infrastructure, dependencies, or release gates.
- Identify MDR, ISO, FDA, SOP, tenant-isolation, RBAC, audit, or enterprise-governance implications when relevant.
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Build a validation matrix.
- Select unit, integration, regression, API, smoke, snapshot, load, mutation, compliance, and security tests according to risk.
- Include mock or synthetic test data requirements.
- Add canary, rollback, runtime, and performance-regression checks for production-facing changes.
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Run security and compliance review.
- Check secrets, dependency risk, license risk, supply-chain exposure, container security, policy enforcement, prompt isolation, and runtime permissions.
- Validate PII redaction, least privilege, tenant isolation, sandbox execution, and audit-trail requirements.
- Treat automated findings as evidence to triage, not as a substitute for reasoning.
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Document audit evidence.
- Record decisions, controls, tests, residual risks, and approval gates.
- Preserve traceability from requirement to implementation to validation result.
- Produce clear review notes for teams, PRs, and regulated approval workflows.
Feature Coverage
- Unit, integration, regression, smoke, snapshot, load, mutation, and compliance test generation
- Static analysis, dependency validation, container checks, supply-chain security, license analysis, and runtime validation
- AI-assisted bug reproduction, test-impact analysis, intelligent failure correlation, and test repair
- RBAC, Entra ID, least privilege, sandboxing, secret isolation, policy engine, approval gates, tenant isolation, and zero-trust controls
- MDR, ISO, FDA, SOP, audit export, revision-safe logs, governance dashboards, and compliance reporting
Output Shape
Return a concise governance report:
- Risk classification
- Required checks
- Evidence collected
- Findings by severity
- Approval gates
- Residual risk