14 件 ・ 関連度順
概要と使いどころ
Use this skill when the user asks about US-Canada cross-border CMV operations — CVOR (Commercial Vehicle Operator's Registration), NSC (National Safety Code), Ontario / Quebec / BC specific rules, US carrier obtaining Canadian operating authority, FAST card for drivers, customs (CBSA), Health Canada hazmat, and how Transport Canada equivalents differ from US FMCSA. Reference USMCA + Transport Canada NSC 14.
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。
Guides compliance with Canada's Personal Information Protection and Electronic Documents Act (PIPEDA, S.C. 2000, c. 5). Covers the 10 fair information principles in Schedule 1, consent requirements, cross-border transfer obligations, breach notification under Division 1.1, and OPC enforcement. Keywords: PIPEDA, Canada privacy, fair information principles, OPC, breach notification, cross-border transfer, consent.
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。
Run an attorney-facing knockout/availability trademark search across the United States and Canada. Use whenever a user (founder, client, or attorney) asks whether a brand, mark, name, logo, slogan, or product name is "available," "free to use," "clearable," or "already taken" — or asks Claude to "search the trademark register," "check USPTO," "check CIPO," "do a knockout search," "clearance search," "availability search," or "see if [mark] is trademarked." Trigger even when the user phrases it casually ("can I call my company X?", "is this name taken?"). Covers federal USPTO (TESS/TSDR), federal Canada (CIPO), common-law/web/state, and WIPO Madrid international. Output is a knockout availability memo with green/yellow/red verdict for attorney review. Includes professional-responsibility gating (AI-use disclosure, conflict check, scope confirmation) before substantive analysis. Not legal advice — produces work product for attorney sign-off.
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。
Creates demand generation campaigns, optimizes paid ad spend across LinkedIn, Google, and Meta, develops SEO strategies, and structures partnership programs. Use when planning demand gen strategy, growth marketing, advertising campaigns, PPC optimization, lead generation, pipeline generation, or marketing budgets. Covers multi-channel acquisition (Google Ads, LinkedIn Ads, Meta Ads), CAC analysis, MQL/SQL workflows, attribution modeling, technical SEO, and co-marketing partnerships. Default calibration profile is a Series A+ B2B SaaS scaling internationally (EU/US/Canada, hybrid PLG/Sales-Led) — adapt benchmarks for other stages and motions rather than skipping the skill.
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。
Pay-per-call access to the Hexanon family of eight x402 APIs for autonomous agents — no signup, no API keys, USDC on Base. Covers US/Canada vehicle & VIN intelligence (Vindex), e-commerce demand signals (Demandex), Polymarket whale intelligence (OrcaTrace), GitHub trending-repo digests (gitBeacon), narrative intelligence (Signalis), Moltbook community digests (Moltalyzer), x402 seller conformance scanning (x402lint), and Polymarket weather-market signals (Isocast).
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。
Drafts formal explanation letters for Canadian Study Permit applications by structuring the argument around program attractiveness, background relevance, choice rationale, and family benefits.
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。
Mark Glazebrook (Dalhousie University, Canada) 视角. 跟腱病 PhD + 关节镜专家 + COA 前主席. 调用此 skill 时, 用 Glazebrook 框架做跟腱病变 / 关节镜 / 循证治疗等级决策.
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。
Your Personal Finance Manager for Canadians — an AI financial planning partner that conducts thorough financial interviews, builds complete plans, generates interactive dashboards, and provides ongoing coaching. Use this skill whenever someone asks about budgeting, saving, investing, debt strategy, retirement planning, tax optimization, government benefits, insurance, RRSPs, TFSAs, RESPs, CPP, OAS, or any aspect of personal finance in a Canadian context. Also triggers for "should I buy this?", "can I afford this?", financial check-ins, plan updates, life change impacts on finances, or any request to build or review a financial plan. Even if the user just says "help me with my money" or "I need a budget", this skill should activate. Canada-focused.
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。
Creates demand generation campaigns, optimizes paid ad spend across LinkedIn, Google, and Meta, develops SEO strategies, and structures partnership programs for Series A+ startups scaling internationally. Use when planning marketing strategy, growth marketing, advertising campaigns, PPC optimization, lead generation, pipeline generation, or startup marketing budgets. Covers multi-channel acquisition (Google Ads, LinkedIn Ads, Meta Ads), CAC analysis, MQL/SQL workflows, attribution modeling, technical SEO, and co-marketing partnerships for hybrid PLG/Sales-Led motions in EU/US/Canada markets.
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。
Drafts USMCA/NAFTA Certificates of Origin for preferential tariff treatment on US-Mexico-Canada goods. Verifies origin criteria, HS classifications, and regional value content. Use when preparing trade certificates, customs origin documentation, duty preference claims, or cross-border shipment certifications.
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。
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.
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。
Bring an EPA SWMM (.inp) or EPANET (.inp) model into MIKE+ via the mike-plus MCP server — the bridge from an INP builder such as SWMMCanada or agentic-swmm into a MIKE+ database that mike_model_info / mike_run can use. Use when the user has an .inp and wants it in MIKE+. Requires MIKE+ installed + a checked-out license (demo mode caps the model size).
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。
Drafts formal explanation letters for Canadian Study Permit applications by structuring the argument around program attractiveness, background relevance, choice rationale, and family benefits.
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。