基于《广告法》《电子商务法》《消费者权益保护法》及司法解释，结合食品、化妆品、医疗器械、纺织、玩具、电子产品等领域实务案例，从广告合规与消费者权益保护角度提供专业意见。当用户提到广告合规审查、广告违法风险、广告违禁词、虚假宣传、消费者权益、惩罚性赔偿、知假买假、商品标签合规、商标侵权风险、电商详情页审查、行政处罚风险、职业打假、消保咨询、文案合规改写等场景时使用本技能。
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Drafts U.S. commercial real estate access and indemnity (right-of-entry) agreements for pre-closing due diligence. Covers license grants, non-invasive vs invasive testing gates, insurance/endorsement requirements, indemnity with discovery carve-outs, restoration and lien remedies, confidentiality, and anti-indemnity guardrails. Trigger: access agreement, right of entry, due diligence access, Phase I/II, invasive testing, pre-PSA site inspection.
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本技能构建 AI 辅助任务的结构化审计轨迹：工具被要求做什么、提供了什么材料、产出了什么、输出如何被验证、最终依赖了什么。它记录工作流以供监督和日后审查，不就特权或披露作出裁定，因此记录保持准确而非自我服务。
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欧盟 AI 法案知识引擎——以 70 份官方欧盟来源文件为基础的权威监管问答（包括 2026 年委员会关于 Art. 6 高风险分类的指南草稿——一般原则、附件 I、附件 III）。基于完整条例文本、委员会指南、EDPB/EDPS 意见、《实践守则》、协调标准、FRIA 指南、事件模板和行业特定指引，以条款级引用回答关于 AI 法案的任何问题。当用户询问"EU AI Act"、"AI Act regulation"、"Regulation 2024/1689"、"KI-Verordnung"、要求"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"，或任何关于欧盟人工智能监管的问题时，应使用本技能。德语术语同样触发："KI-Gesetz"、"KI-Verordnung"、"Hochrisiko-KI"、"KI-Kompetenz"、"Grundrechte-Folgenabschaetzung"、"GPAI-Verhaltenskodex"。对于产出分类决定而非知识答案的评估工作流，提议在会话内运行结构化风险等级分类。
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Agent 专用邮箱统一管理：让 Claude Code、Codex 等平台的 Agent 用一套命令收发邮件、整理收件箱、分发任务。支持网易 ClawEmail（claw.163.com）和腾讯 Agent Mail（QQ 邮箱，agent.qq.com）两家后端，通过 MAIL_PROVIDER 切换。当用户提到收发邮件、看收件箱、搜索邮件、回复转发邮件、下载附件、整理邮件、给其他 Agent 派邮件任务、配置 Agent 邮箱、腾讯 QQ 邮箱 Agent、网易 ClawEmail 时使用此 skill。
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在部署前为企业或受监管的 AI 智能体创建《智能体权限宪章》（Agent Authority Charter）。当用户需要界定 AI 智能体被允许做什么、谁向其授予了权限、哪些行动被允许或禁止、何时需要人工批准、必须保留哪些证据，以及智能体如何被暂停、撤销或升级时，使用本技能。
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Drafts U.S. regulatory client advisory summaries translating legal developments into actionable risk and compliance guidance. Use when a client needs a proactive memo, client alert, or legal-update brief for a new law, case, rulemaking, agency guidance, or pending reform. Trigger on requests for "client advisory," "regulatory update," "legal alert," "compliance briefing," "new law summary," or "quarterly advisory."
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Drafts adverse possession complaints and quiet title pleadings. Structures jurisdictional foundations, legal property descriptions, and element-by-element proof of actual, open, continuous, exclusive, and hostile possession. Use when filing adverse possession claims, quiet title actions, or prescriptive ownership pleadings.
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Drafts an Adverse Event Reporting Policy compliant with 21 CFR 312.32 (IND safety reporting), 21 CFR 314.80 (postmarketing), and ICH E2A, with multi-jurisdictional overlays (EMA, PMDA, Health Canada). Covers seriousness/causality frameworks, expedited reporting timelines, roles, documentation standards, training mandates, and QA mechanisms. Use when drafting or updating an adverse event reporting policy, pharmacovigilance policy, AE/SAE reporting SOP, or safety reporting framework for a pharmaceutical company, CRO, biotech, or clinical research institution.
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Drafts adversary proceeding complaints for U.S. Bankruptcy Court under FRBP Rule 7001. Covers dischargeability disputes (§ 523), preference actions (§ 547), fraudulent transfers (§ 548), and stay violations (§ 362). Produces a filing-ready pleading with caption, jurisdictional basis, numbered allegations, count structure, and prayer for relief. Triggers when a trustee, creditor, or party in interest needs to initiate litigation within an existing bankruptcy case.
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Drafts jurisdiction-specific Advance Health Care Directive packages with agent appointment, living will instructions, HIPAA authorization bridge, organ donation preferences, and execution compliance checklists. Trigger when the user mentions advance directive, healthcare proxy, living will, health care agent, HIPAA authorization, medical power of attorney, end-of-life planning, capacity trigger planning, state-specific directive forms, witness/notary requirements for healthcare documents, or cross-state directive portability.
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Manages Rule 30(b)(6) corporate representative deposition workflows — drafting notice topics with reasonable particularity, building examination outlines, defending designees, handling objections, and preserving binding admissions for summary judgment or trial. Use when drafting or responding to 30(b)(6) notices, selecting and preparing designees, building topic-by-topic outlines, or triaging scope and privilege disputes. Trigger keywords: 30(b)(6), corporate representative deposition, topic list, designee, notice analysis, deposition objections, corporate admissions.
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AI compliance and policy engine — evaluate scan results against OWASP, NIST, SOC 2, ISO 27001, CMMC, EU AI Act, AISVS v1.0, and related frameworks. Generate SBOMs and compliance reports. Use when: "compliance report", "NIST", "SOC 2", "ISO 27001", "OWASP", "EU AI Act", "AISVS", "generate SBOM", "policy check".
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