EU AI Act (Regulation (EU) 2024/1689) Article-cited compliance operator. Three decisions: AI system risk tier (Article 5 / 6+ Annex III / 50 / minimal), conform
所属插件包：compliance-os
ISO/IEC 42001:2023 AI Management System (AIMS) implementation + internal audit operator. Three decisions: AIMS gaps against Clauses 4-10, AI risk register per A
所属插件包：compliance-os
ISO/IEC 27001:2022 ISMS audit + implementation persona. Sample-driven; samples real records, not curated demos. Coordinates with SOC 2 (75% overlap), ISO 42001
所属插件包：compliance-os
Multi-framework compliance officer orchestrating cross-framework programs. Routes per-framework deep work to specialist skills (ISO 42001, EU AI Act, ISO 27001,
所属插件包：compliance-os
ISO 13485:2016 QMS audit persona — Design Control + CAPA + Process Validation focused. Coordinates with ISO 14971 (risk file), MDR 745 (technical documentation)
所属插件包：compliance-os
GDPR / DSGVO Data Protection Officer audit persona. Lawful-basis-discipline + DPIA-quality + Schrems-II-transfer-aware. Coordinates with ISO 27001 Article 32 or
所属插件包：compliance-os
FDA 21 CFR 820 (QSR / QMSR) auditor persona. Substantially harmonized with ISO 13485 post-Feb 2026 via FDA Final Rule incorporating ISO 13485 by reference. Adds
所属插件包：compliance-os
SOC 2 Type II auditor persona — observation-period discipline + AICPA TSC focused. Coordinates with ISO 27001 (75% overlap, the canonical cross-walk pair) and G
所属插件包：compliance-os
/cs:ai-act-readiness <system> — EU AI Act 6-question forcing interrogation. Use during AI-system intake, before EU deployment, or during annual compliance refre
所属插件包：compliance-os
/cs:aims-audit <scope> — ISO/IEC 42001 AIMS internal-audit 6-question forcing interrogation. Use before certification stage 1, before annual internal audit cycl
所属插件包：compliance-os
Compliance OS — meta-orchestrator that lets compliance teams CONFIGURE which frameworks apply, COMPUTE cross-framework control overlap, SIMULATE internal audits
所属插件包：compliance-os
/cs:compliance-readiness <program> — Multi-framework compliance officer 6-question forcing interrogation of any compliance program. Use before starting a new fr
所属插件包：compliance-os
/cs:fda-qsr-audit-prep <scope> — FDA 21 CFR 820 (QSR / QMSR) audit 6-question forcing interrogation. Post-Feb 2026 substantially harmonized with ISO 13485. Use
所属插件包：compliance-os
/cs:gdpr-audit-prep <scope> — GDPR audit 6-question Article-cited forcing interrogation. Use before annual internal GDPR review, post-breach internal audit, DPA
所属插件包：compliance-os
/cs:iso13485-audit-prep <scope> — ISO 13485 QMS audit 6-question forcing interrogation. Design controls + CAPA + post-market focused. Use before Clause 8.2.4 in
所属插件包：compliance-os
/cs:iso27001-audit-prep <scope> — ISO 27001 ISMS audit readiness 6-question forcing interrogation. Use before annual Clause 9.2 internal audit, surveillance aud
所属插件包：compliance-os
/cs:soc2-audit-prep <scope> — SOC 2 Type II readiness 6-question forcing interrogation. Observation-period focused. Use before Type II observation begins, mid-p
所属插件包：compliance-os
