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概要と使いどころ
Builds a structured ransomware incident response playbook aligned with the CISA StopRansomware Guide and NIST Cybersecurity Framework, covering preparation, detection, containment, eradication, recovery, and post-incident phases with actionable checklists. Use when creating or updating a ransomware playbook, running a CISA-aligned readiness assessment, or validating response steps during a tabletop exercise.
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。
Parses Software Bill of Materials (SBOM) in CycloneDX and SPDX JSON formats to identify supply chain vulnerabilities by correlating components against the NVD CVE database via the NVD 2.0 API. Builds dependency graphs, calculates risk scores, identifies transitive vulnerability paths, and generates compliance reports. Activates for requests involving SBOM analysis, software composition analysis, supply chain security assessment, dependency vulnerability scanning, CycloneDX/SPDX parsing, or CVE correlation.
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。
Installs and runs the kube-bench tool against a Kubernetes cluster as a Job, DaemonSet, or standalone binary, selecting the correct benchmark version and targets (control plane, etcd, kubelet, worker nodes) and emitting JSON or JUnit output for pipelines. Use when setting kube-bench up for the first time, choosing which benchmark version and node targets to run, wiring it into CI, or troubleshooting skipped or misdetected checks. Keywords: kube-bench, DaemonSet, --benchmark, --targets, JSON output, JUnit, CI integration. Do not use for interpreting the findings or producing an audit report - use performing-kubernetes-cis-benchmark-with-kube-bench.
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。
Project architecture and file structure conventions for all process types. Use when: (1) Creating new files or modules, (2) Deciding where code should go, (3) Converting single-file components to directories, (4) Reviewing code for structure compliance, (5) Adding new bridges, services, agents, or workers.
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。
Internationalization (i18n) workflow and standards for managing translations. Use when: (1) Adding new user-facing text, (2) Creating new components with user-facing text, (3) Reviewing code for i18n compliance, (4) Adding a new translation module.
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。
Audit and improve web accessibility following WCAG 2.1 guidelines. Use when asked to "improve accessibility", "a11y audit", "WCAG compliance", "screen reader support", "keyboard navigation", or "make accessible".
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。
Review UI code for Web Interface Guidelines compliance. Use when asked to "review my UI", "check accessibility", "audit design", "review UX", or "check my site against best practices".
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。
Review UI code for Web Interface Guidelines compliance. Use when asked to "review my UI", "check accessibility", "audit design", "review UX", or "check my site against best practices".
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。
Review docs/prose for Writing Guidelines compliance. Use when asked to "review my docs", "check writing style", "audit prose", "review docs voice and tone", or "check this page against the writing handbook".
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。
审计、修复并验证 TradingAgentsCN 中 agent 与提示词工作流。用于持仓分析、workflow prompt、MongoDB prompt_templates、adapter prompt assembly、合规修复、运行期模板与代码同步。触发词：修改 agent 提示词、提示词治理、DB 模板同步、workflow 提示词修复、持仓分析提示词排查、prompt compliance、runtime prompt audit。
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 this skill to create fillable Word forms (.docx) with real Content Controls (SDT) + legacy FormField checkboxes + MERGEFIELD mail-merge placeholders + document protection. Trigger on: 'fillable form', 'form fields', 'content controls', 'SDT', 'word form', 'fill in', 'only editable fields', 'protect document', 'onboarding form', 'HR intake', 'survey template', 'contract / SOW template', 'mail-merge template', 'compliance checklist', 'medical intake questionnaire'. Output is a single .docx where specific fields are editable and the rest is locked. This skill is INDEPENDENT, not a scene layer on docx — payload is `w:sdt` + `w:ffData` + `w:fldChar` + `documentProtection`, none of which docx base skill covers. Do NOT trigger for regular reports, letters, memos, academic papers, pitch decks, or any document with no user-fillable fields — route those to officecli-docx or its scene layers.
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。
Prepare structured briefings for meetings with legal relevance and track resulting action items. Use when preparing for contract negotiations, board meetings, compliance reviews, or any meeting where legal context, background research, or action tracking is needed.
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。
Support SOX 404 compliance with control testing methodology, sample selection, and documentation standards. Use when generating testing workpapers, selecting audit samples, classifying control deficiencies, or preparing for internal or external audits.
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。
Router/index for the 15 regulatory & quality-management skills bundled in this plugin (ISO 13485 QMS, EU MDR 2017/745, FDA submissions under QMSR, ISO 14971 risk, CAPA, document control, ISO 27001/ISMS, ISO 42001 AIMS, EU AI Act, GDPR/DSGVO, SOC 2, auditing). Use when a compliance request doesn't obviously match one skill and you need to pick the right one (e.g., 'prepare us for an ISO 13485 audit', 'is my AI system high-risk 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。
FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QMSR (21 CFR 820, which incorporates ISO 13485:2016 by reference since 2026-02-02; formerly QSR) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QMSR, QSR, ISO 13485 for FDA, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.
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 MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, Art. 86 PSUR schedules, and EUDAMED integration. Use when classifying a medical device under MDR, building or gap-checking a technical file, planning clinical evaluation or PMS/PSUR cadence, or preparing for notified body review (e.g., 'what class is my device under MDR', 'review my PSUR schedule').
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。
Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathways for new medical devices; drafts responses to FDA deficiency letters and Notified Body queries; develops CE marking technical documentation under EU MDR 2017/745; coordinates multi-market approval strategies across FDA, EU, Health Canada, PMDA, and NMPA; and maintains regulatory intelligence on evolving standards. Use when users need to plan or execute FDA submissions, navigate 510(k) or PMA approval processes, achieve CE marking, prepare pre-submission meeting materials, write regulatory strategy documents, respond to agency queries, or manage compliance documentation for medical device market access.
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 27001 ISMS implementation and cybersecurity governance for HealthTech and MedTech companies. Use when designing an ISMS, running security risk assessments, implementing controls, pursuing ISO 27001 certification, preparing security audits, responding to security incidents, or verifying compliance. Covers ISO 27001, ISO 27002, healthcare security, and medical device cybersecurity.
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 the user asks to prepare for SOC 2 audits, map Trust Service Criteria, build control matrices, collect audit evidence, perform gap analysis, or assess SOC 2 Type I vs Type II readiness.
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。
Senior Quality Manager Responsible Person (QMR) for HealthTech and MedTech companies. Provides quality system governance, management review leadership, regulatory compliance oversight, and quality performance monitoring per ISO 13485 Clause 5.5.2. Use when leading management reviews, setting quality policy and objectives, monitoring quality KPIs and cost of quality, or exercising QMR governance and regulatory oversight responsibilities.
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。
Information Security Management System (ISMS) audit expert for ISO 27001 compliance verification, security control assessment, and certification support. Use when the user mentions ISO 27001, ISMS audit, Annex A controls, Statement of Applicability (SOA), gap analysis, nonconformity management, internal audit, surveillance audit, or security certification preparation. Helps review control implementation evidence, document audit findings, classify nonconformities, generate risk-based audit plans, map controls to Annex A requirements, prepare Stage 1 and Stage 2 audit documentation, and support corrective action workflows.
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。
Audit and manage dependencies across multi-language projects. Identifies vulnerabilities, license conflicts, transitive dependency risks, and safe-upgrade paths. Use when auditing third-party packages before release, investigating a CVE, planning a major version bump, or running a license-compliance review. Examples: 'audit our npm dependencies', 'do we have GPL contamination', 'plan the upgrade to React 19'.
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。
Microsoft 365 tenant administration for Global Administrators. Automate M365 tenant setup, Office 365 admin tasks, Azure AD user management, Exchange Online configuration, Teams administration, and security policies. Generate PowerShell scripts for bulk operations, Conditional Access policies, license management, and compliance reporting. Use for M365 tenant manager, Office 365 admin, Azure AD users, Global Administrator, tenant configuration, or Microsoft 365 automation.
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。