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Found 1,487 Skills
Stage 1 spec compliance review. Triggers: /review stage 1. Verifies implementation matches design specification — functional completeness, TDD compliance, and test coverage. Do NOT use for code quality checks — use quality-review instead. Do NOT use for debugging.
Scan project dependencies for CVEs, outdated packages, and license compliance across npm, pip, cargo, go, maven, and other ecosystems. Use for vulnerability scanning, SBOM generation, supply chain analysis, and automated dependency updates.
Guides compliance with Brazil's Lei Geral de Proteção de Dados (LGPD, Lei 13.709/2018). Covers the 10 lawful bases under Art. 7, DPO appointment, ANPD enforcement, data subject rights under Arts. 17-22, and international transfer mechanisms. Keywords: LGPD, Brazil data protection, ANPD, lawful bases, data subject rights, international transfers.
This skill should be used when the user asks to draft or structure STR reports, suspicious transaction reports, SAR, suspicious activity reports, draft STR, STR narrative, file suspicious activity, AML STR, goAML, FinCEN SAR, suspicion narrative, or MLRO report. Guides jurisdiction-agnostic STR/SAR drafting—narrative structure (who, what, when, where, why suspicious), red flags and typologies, transaction aggregation and chronology, subject identification fields, supporting documentation checklists, quality review before filing, and escalation to MLRO/compliance—not TM rule building (aml-compliance), full LE case management, legal filing duty determination (commercial-counsel), or deep blockchain tracing (blockint skills). Complements aml-compliance, aml-cft, auditor, compliance-engineer, and commercial-counsel.
Senior FDA consultant and specialist for medical device companies including HIPAA compliance and requirement management. Provides FDA pathway expertise, QSR compliance, cybersecurity guidance, and regulatory submission support. Use for FDA submission planning, QSR compliance assessments, HIPAA evaluations, and FDA regulatory strategy development.
FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QSR (21 CFR 820) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QSR, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.
Audit code comments and docstrings quality across 6 categories (WHY-not-WHAT, Density, Forbidden Content, Docstrings, Actuality, Legacy). Use when code needs comment review, after major refactoring, or as part of ln-100-documents-pipeline. Outputs Compliance Score X/10 per category + Findings + Recommended Actions.
Build accessible UIs with semantic HTML, ARIA attributes, keyboard navigation, color contrast, and screen reader support. Apply when creating or modifying frontend components, forms, interactive elements, or any UI that needs WCAG compliance.
Expert-level construction management, project planning, BIM, safety compliance, and construction technology
Validates CloudFormation templates for syntax, security, and best practices. Use when validating CloudFormation templates, checking for security issues, or ensuring compliance with best practices.
AI governance and compliance guidance covering EU AI Act risk classification, NIST AI RMF, responsible AI principles, AI ethics review, and regulatory compliance for AI systems.
Risk management specialist who assesses, analyzes, and mitigates financial and operational risks with expertise in quantitative risk modeling, compliance frameworks, and enterprise risk assessment