32 件 ・ 関連度順
概要と使いどころ
/cs:ai-act-readiness <system> — EU AI Act 6-question forcing interrogation. Use during AI-system intake, before EU deployment, or during annual compliance refresh as Article 113 obligations phase in (2025-02-02 / 2025-08-02 / 2026-08-02 / 2027-08-02).
日本語の概要は準備中です。原文の説明を表示しています。
EU AI Act (Regulation EU 2024/1689) compliance specialist. Use for AI system risk classification, provider/deployer obligations, GPAI model compliance, conformity assessments, bias and fairness testing, and AI governance programs.
日本語の概要は準備中です。原文の説明を表示しています。
Preparing EU AI Act compliance documentation for high-risk AI systems. Covers Annex III classification, technical documentation under Art. 11, conformity assessment, risk management systems, and CE marking requirements. Keywords: EU AI Act, high-risk AI, Annex III, conformity assessment, CE marking.
日本語の概要は準備中です。原文の説明を表示しています。
/cs:ai-act-readiness <system> — EU AI Act 6-question forcing interrogation. Use during AI-system intake, before EU deployment, or during annual compliance refresh as Article 113 obligations phase in (2025-02-02 / 2025-08-02 / 2026-08-02 / 2027-08-02).
日本語の概要は準備中です。原文の説明を表示しています。
/cs:ai-act-readiness <system> — EU AI Act 6-question forcing interrogation. Use during AI-system intake, before EU deployment, or during annual compliance refresh as Article 113 obligations phase in (2025-02-02 / 2025-08-02 / 2026-08-02 / 2027-08-02).
日本語の概要は準備中です。原文の説明を表示しています。
EU AI Act (Regulation (EU) 2024/1689) operational compliance for compliance teams. Three Article-level decisions: (1) What's the risk tier of this AI system — prohibited (Art. 5), high-risk (Art. 6 + Annex III), limited-risk (Art. 50), or minimal-risk? (2) For high-risk systems, what's the Article 43 conformity assessment route (Module A internal control vs Module H full QMS + notified body) and what goes in the Annex IV technical documentation? (3) Per organizational role (provider / deployer / importer / distributor / authorized representative), what are the active obligations and deadlines? Use during AI system intake review, when planning conformity assessment, or when scoping deployer obligations. Cites Articles + Annexes for every output. NOT executive AI strategy (see chief-ai-officer-advisor). NOT a legal substitute.
日本語の概要は準備中です。原文の説明を表示しています。
ISO/IEC 42001:2023 AI Management System (AIMS) specialist for compliance teams running internal audits. Three decisions: (1) Where are the gaps against Clauses 4-10 and what do we close first? (2) What goes in the AI risk register and which Annex A controls treat each risk? (3) What's the 12-month internal audit plan that satisfies Clause 9.2? Use when preparing for certification, scoping internal audit cycles, or onboarding AI systems into an existing ISMS (27001) / QMS (13485) program. NOT an executive AI strategy skill (see chief-ai-officer-advisor). NOT EU AI Act compliance (see compliance-team-eu-ai-act).
日本語の概要は準備中です。原文の説明を表示しています。
EU AI Act (Regulation (EU) 2024/1689) compliance advisor — risk classification across all four tiers, all 9 prohibited practices (Art. 5, including the nudification/CSAM prohibition from Dec 2, 2026), all 8 Annex III high-risk use case areas, provider and deployer obligations (Arts. 9–17, 26), GPAI model obligations including the July 2025 Code of Practice (Arts. 51–55), conformity assessment and CE marking (Arts. 43–48), EU AI database registration, Art. 50 transparency (chatbots, synthetic media, AI-generated content), governance (AI Office, AI Board), penalties (Art. 99), confirmed phase-in timeline (Digital Omnibus, Reg. (EU) 2026/1744, in force July 27, 2026: Annex III deferred to Dec 2, 2027; Annex I to Aug 2, 2028), and cross-framework mapping to ISO 42001, NIST AI RMF, and GDPR. Use for any EU AI regulation, AI system classification, or AI compliance question. Current as of August 2026. GPAI enforcement powers active since August 2, 2026.
日本語の概要は準備中です。原文の説明を表示しています。
Check AI-generated marketing content and reviews for required disclosures under the EU AI Act, FTC rules and platform AI-label policies. Use when labelling AI ads, deepfakes, chatbots, influencer posts or testimonials.
日本語の概要は準備中です。原文の説明を表示しています。
Determines the organization's role (provider, deployer, importer, distributor, or quasi-provider) and assesses Art. 25 quasi-provider risk of the EU AI Act. This skill should be used when the user asks to "determine AI Act roles", "check if we are provider or deployer", "assess quasi-provider status", "check Art. 25 substantial modification", "check value chain responsibilities", or mentions "Betreiber", "Anbieter", "wesentliche Veränderung", or finetuning implications under the AI Act.
日本語の概要は準備中です。原文の説明を表示しています。
Fast 15-25 minute triage for preliminary EU AI Act classification and compliance assessment. This skill should be used when the user asks to "do a quick AI Act assessment", "check if the AI Act applies to us", "run a preliminary classification", "do an AI Act triage", "quick check", "preliminary assessment", "Schnellprüfung", "Ersteinschätzung", or needs a fast initial assessment before committing to full analysis.
日本語の概要は準備中です。原文の説明を表示しています。
Maps the full set of legal obligations for the EU AI Act based on role + risk tier, producing an actionable compliance matrix with RACI assignments and implementation priorities. This skill should be used when the user asks to "map AI Act obligations", "check what we need to do under the AI Act", "create a compliance checklist", "check deployer obligations", "assess provider duties", or mentions Art. 26, Art. 16-17, AI literacy Art. 4, DPIA, fundamental rights assessment, or "Pflichtenkatalog" under the AI Act.
日本語の概要は準備中です。原文の説明を表示しています。
Assess whether a Fundamental Rights Impact Assessment (FRIA) is required under Article 27 EU AI Act, and structure or draft that assessment for a specific high-risk AI deployment. Covers deployer scope gating (public bodies and private entities providing public services), affected group mapping, Charter rights analysis, proportionality, safeguards evaluation, residual risk, DPIA/FRIA cross-referencing under the amended Article 27(4), the unconditional notification duty under Article 27(3), and DACH-specific considerations. Use when asked about FRIA obligations, Article 27 scope, fundamental rights and AI, or deployer assessment duties.
日本語の概要は準備中です。原文の説明を表示しています。
Assess and operationalize implementation readiness for high-risk AI systems under the EU AI Act Annex III, including provider and deployer obligations, conformity assessment, post-market monitoring, and EU database registration. Use when users say things like “we classified this as high-risk, what now?”, “build an EU AI Act readiness plan”, “assess our Annex III compliance gaps”, “what do providers/deployers of high-risk AI need to implement?”, “prepare for conformity assessment”, or “create a high-risk AI implementation roadmap.”
日本語の概要は準備中です。原文の説明を表示しています。
Depth assessment of whether an AI system is high-risk under Art. 6 of the EU AI Act, grounded in the Commission's draft Art. 6(5) classification guidelines (general principles + Annex I + Annex III). Covers the Annex I product-safety route, all eight Annex III areas with worked examples, the Art. 6(3) exception and its profiling re-exception, and the Art. 25 quasi-provider trap. Outputs a structured decision block, a practitioner memo, and a JSON interchange artefact.
日本語の概要は準備中です。原文の説明を表示しています。
Generates a formal, structured AI Act compliance assessment report suitable for legal files, audit trails, and regulatory inquiries. This skill should be used when the user asks to "generate an AI Act report", "create a compliance assessment report", "document the AI Act analysis", "create a Prüfbericht", "export as Word document", or wants to consolidate prior AI Act skill outputs into a formal documented assessment.
日本語の概要は準備中です。原文の説明を表示しています。
EU AI Act Knowledge Engine — authoritative regulatory Q&A grounded in 70 official EU source documents (including the 2026 Commission draft guidelines on Art. 6 high-risk classification — general principles, Annex I, Annex III). Answers any question about the AI Act with article-level citations from the full regulation text, Commission guidelines, EDPB/EDPS opinions, codes of practice, harmonised standards, FRIA guides, incident templates, and sector-specific guidance. This skill should be used when the user asks about the "EU AI Act", "AI Act regulation", "Regulation 2024/1689", "KI-Verordnung", asks to "explain an AI Act article", "what does Article X say", "AI Act requirements", "AI Act penalties", "AI Act timeline", "GPAI obligations", "high-risk AI", "prohibited AI practices", "AI Act and GDPR", "fundamental rights impact assessment", "AI Act standards", "AI Act national implementation", "AI literacy", "serious incident reporting", "Digital Omnibus", "AI regulatory sandbox", or any question about EU artificial intelligence regulation. Also triggers on German terms: "KI-Gesetz", "KI-Verordnung", "Hochrisiko-KI", "KI-Kompetenz", "Grundrechte-Folgenabschaetzung", "GPAI-Verhaltenskodex". For assessment workflows that produce a classification decision rather than a knowledge answer, offer to run a structured risk-tier classification in-session.
日本語の概要は準備中です。原文の説明を表示しています。
Assesses which of the Art. 50(1)-(5) transparency obligations of the EU AI Act apply to a given AI system's provider or deployer, grounded in the final Code of Practice on Transparency of AI-Generated Content (June 2026) and the Commission's draft Art. 50 Guidelines. Covers AI-chatbot disclosure, deepfake and synthetic-content marking/watermarking, emotion-recognition and biometric-categorisation notices, the machine-readable marking duty, the obviousness exceptions, and the implementation timeline. Outputs a formal mini-report plus a per-obligation compliance checklist with gap flags. For breadth-first tier triage use the EU AI Act System Classifier; for raw Art. 50 text and Q&A use the EU AI Act Knowledge Base; for the full role x tier matrix use the EU AI Act Obligations Mapper.
日本語の概要は準備中です。原文の説明を表示しています。
EU AI Act (Regulation (EU) 2024/1689) compliance advisor — risk classification across all four tiers, all 9 prohibited practices (Art. 5, including the nudification/CSAM prohibition from Dec 2, 2026), all 8 Annex III high-risk use case areas, provider and deployer obligations (Arts. 9–17, 26), GPAI model obligations including the July 2025 Code of Practice (Arts. 51–55), conformity assessment and CE marking (Arts. 43–48), EU AI database registration, Art. 50 transparency (chatbots, synthetic media, AI-generated content), governance (AI Office, AI Board), penalties (Art. 99), confirmed phase-in timeline (Digital Omnibus adopted June 29, 2026: Annex III deferred to Dec 2, 2027; Annex I to Aug 2, 2028), and cross-framework mapping to ISO 42001, NIST AI RMF, and GDPR. Use for any EU AI regulation, AI system classification, or AI compliance question. Current as of July 2026. GPAI enforcement powers activate August 2, 2026.
日本語の概要は準備中です。原文の説明を表示しています。
Classify AI systems under the EU AI Act (Regulation (EU) 2024/1689) and determine compliance obligations. Use when asked to assess AI risk level, check if an AI system is prohibited, determine high-risk status, identify GPAI model obligations, map provider/deployer responsibilities, or build an AI Act compliance roadmap. Covers the full classification decision tree (Prohibited → High-Risk → Limited → Minimal → GPAI), obligations by role (provider, deployer, importer, distributor), compliance timelines, and DACH-specific considerations (German works council, BaFin, BSI, BNetzA). Triggers on phrases like "classify this AI system", "is this high-risk under the AI Act", "AI Act risk assessment", "EU AI Act compliance", "prohibited AI practice", "GPAI obligations", "AI Act timeline".
日本語の概要は準備中です。原文の説明を表示しています。
Determines whether a technology qualifies as an AI system under Art. 3(1) of the EU AI Act and classifies its risk tier (prohibited, high-risk, GPAI with systemic risk, limited risk, minimal risk). This skill should be used when the user asks to "classify an AI system under the AI Act", "determine the AI Act risk tier", "check if something is an AI system", "assess prohibited practices", "check high-risk classification", "determine Art. 6 exception applicability", or mentions "KI-Verordnung", "Risikoklassifizierung", Art. 5, Annex III, or GPAI systemic risk.
日本語の概要は準備中です。原文の説明を表示しています。
Use when reviewing, designing, or modifying Java enterprise systems that use AI, LLMs, AI agents, RAG, tool calling, workflow automation, or model-based decision support and need EU AI Act regulatory awareness. This should trigger for requests such as Review a Java AI system for EU AI Act controls; Design governance for an AI agent with enterprise tools; Add human oversight and auditability to LLM workflows; Assess RAG or model-driven decision support before production release. Part of Plinth Toolkit
日本語の概要は準備中です。原文の説明を表示しています。
Check construction AI systems against the EU AI Act (Regulation 2024/1689): classify risk of estimation, scheduling, CV and agent tools, document transparency, keep human oversight. Use when deploying or auditing AI in construction.
日本語の概要は準備中です。原文の説明を表示しています。
Addresses healthcare AI privacy at the intersection of HIPAA and the EU AI Act for clinical decision support systems. Covers training data PHI handling, model transparency and explainability, patient rights in algorithmic decisions, FDA/OCR regulatory coordination, and bias monitoring. Keywords: healthcare AI, HIPAA, AI Act, clinical decision support, PHI training data, model transparency.
日本語の概要は準備中です。原文の説明を表示しています。