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2 packs

Results for “compliance-audit”

16 skills
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mukul975
performing-nist-csf-maturity-assessment
Conduct a maturity assessment against the NIST Cybersecurity Framework (CSF) 2.0, using Implementation Tiers to measure organizational cybersecurity posture and create improvement roadmaps.
24.6k · bundle
snoodleboot-io
compliance-automation
The annual compliance scramble exists because controls are tested once, by
2
aibot88
do
Enforce CLAUDE.md framework compliance. Re-reads rules, displays applicable rules, processes request with full compliance.
3 · bundle
luokai0
code-qc
Runs a structured quality control audit on codebases, covering tests, imports, static analysis, type checking, smoke tests, UI verification, file consistency, and documentation, producing a PASS/WARN/FAIL report.
10 · bundle
nagarenegishi
comment-audit
Audits a repository for comment coverage and brings under-commented source files up to standard, one file at a time, with a resumable tracker.
0
shenxingy
review
Clade coverage-driven project review — walks every VERIFY.md checkpoint, fixes failures in-session, converges when all checkpoints pass. NOT the Claude Code built-in /review (which reviews a single pull request diff) — if the user wants a PR review, route to /review-pr (Clade's PR reviewer) or the CC built-in.
8 · bundle
levicarlosz
gdpr-compliance
Expert GDPR compliance assistant covering all four core workflows: (1) auditing code and systems for GDPR violations, (2) drafting GDPR-compliant documents such as privacy policies, Data Processing Agreements (DPAs), and consent notices, (3) answering GDPR compliance questions with authoritative article citations, and (4) reviewing data flows and PII handling practices. Use this skill whenever the user mentions GDPR, data protection, privacy compliance, lawful basis, data subject rights, DPA, privacy notices, consent management, data breaches, DPIAs, controller/ processor relationships, cross-border data transfers, or any EU/UK data privacy topic. Also trigger for questions like "is this GDPR compliant?", "how do I handle personal data?", "what does a privacy policy need?", or any request involving PII, personal data, or data retention in a regulatory context.
2 · bundle
casemark
itar-tcp
Drafts ITAR Technology Control Plans (TCPs) for managing USML defense articles and technical data under 22 CFR Parts 120-130. Covers DDTC registration, classification, access controls, deemed export prevention, secure handling, training, audits, and incident response. Use when creating or updating export control compliance plans, technology control plans, or DDTC submission documents.
34
thedixitjain
adopt
Brownfield onboarding — audits existing project artifacts for template format compliance (not just existence), classifies gaps by impact, and produces a numbered migration plan. Run this when joining an in-progress project or upgrading from an older template version. Distinct from /project-stage-detect (which checks what exists) — this checks whether what exists will actually work with the template's skills.
2
levicarlosz
iso42001
Expert ISO 42001 AI Management System (AIMS) compliance advisor. Use this skill whenever a user asks about ISO/IEC 42001:2023, AI governance, AI management systems, AI risk assessment, AI system impact assessment, Annex A controls for AI, Statement of Applicability for AI systems, AI policy, responsible AI, AI lifecycle management, AI incident management, AI transparency, AI bias, AI certification readiness, or any topic related to implementing or auditing an AI Management System. Also trigger for questions like "how do I become ISO 42001 certified?", "what controls does ISO 42001 require?", "how do I assess AI risk under 42001?", "what is an AIMS?", or any request involving organisational governance of AI systems, responsible AI frameworks, or AI regulatory compliance aligned to an ISO standard.
2 · bundle
casemark
gmp-sop
Drafts inspection-ready GMP standard operating procedures for regulated manufacturing. Covers document control, role accountability, process controls, deviation/CAPA handling, and records management aligned to FDA CGMP (21 CFR 210/211), Part 11, ICH Q7/Q9/Q10, WHO GMP, PIC/S, and EU GMP. Use when creating or overhauling a GMP SOP, preparing for audits or inspections, or building compliance-ready procedures. Trigger: GMP, SOP, CGMP, 21 CFR 210, 21 CFR 211, Part 11, ICH Q7, ICH Q9, ICH Q10, WHO GMP, PIC/S, EU GMP.
34