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Found 1,476 Skills
Design data architecture at enterprise and solution levels. Cover data mesh, lakehouse, governance, domain-driven design, conceptual/logical/physical data modeling, platform selection, and compliance frameworks. Produce ADRs, data model diagrams, platform comparison matrices, and governance policy templates. Triggers on "design data platform", "choose data warehouse", "data mesh", "lakehouse architecture", "data governance", "data modeling", "platform selection", "data architecture decision", "compliance framework", or "data strategy". For applied AI solution architecture (RAG data plane, embeddings, vector stores in commercial or enterprise products), use applied-ai-architect-commercial-enterprise. For dbt analytics layers and mart delivery, use analytics-data-engineer—not data-architect.
Comprehensive design token system for typography, colors, and theming with WCAG AA compliance, TypeScript types, and framework integration (CSS-in-JS, Tailwind, CSS Variables).
Configure GCP Cloud Audit Logs for compliance. Set up log routing and BigQuery analysis. Use when auditing GCP activity.
Comprehensive paid advertising audit and optimization for any business type. Performs full multi-platform audits (Google Ads, Meta Ads, LinkedIn Ads, TikTok Ads, Microsoft Ads), single-platform deep analysis, conversion tracking health checks, creative quality assessment, budget allocation optimization, bidding strategy evaluation, and compliance verification. Industry detection for SaaS, e-commerce, local service, B2B enterprise, info products, mobile app, real estate, healthcare, finance, and agency. Triggers on: "ads", "PPC", "paid advertising", "Google Ads", "Meta Ads", "Facebook Ads", "LinkedIn Ads", "TikTok Ads", "Microsoft Ads", "Bing Ads", "ad audit", "campaign audit", "ROAS", "conversion tracking", "creative fatigue", "bid strategy".
Полный цикл разработки доработок 1С — от анализа до реализации с БСП compliance. 9 фаз: оценка, discovery, исследование, уточнение, проектирование, ревью плана, реализация, ревью кода, итоги.
Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Provides regulatory strategy development, submission management, pathway analysis, global compliance coordination, and cross-functional team leadership.
Transform UI style requirements into production-ready frontend code with systematic design tokens, accessibility compliance, and creative execution. Use when building websites, web applications, React/Vue components, dashboards, landing pages, or any web UI requiring both design consistency and aesthetic quality.
12 production-ready regulatory affairs and quality management skills for HealthTech/MedTech: ISO 13485 QMS, MDR 2017/745, FDA 510(k)/PMA, ISO 27001 ISMS, GDPR/DSGVO compliance, risk management (ISO 14971), CAPA, document control, and internal auditing. Python tools included (all stdlib-only). Works with Claude Code, Codex CLI, and OpenClaw.
Token and address risk assessment. Use this skill whenever the user asks about token, contract, or address safety. Trigger phrases include: is this token safe, check contract risk, is this address safe, honeypot, rug. MCP tools: info_compliance_check_token_security, info_coin_get_coin_info; Address mode: info_onchain_get_address_info.
Use this skill when managing patents, trademarks, trade secrets, or open-source licensing. Triggers on intellectual property, patents, trademarks, trade secrets, open-source licensing, copyright, IP strategy, license compliance, and any task requiring IP protection or licensing decisions.
Automated accessibility testing with axe-core, Playwright, and jest-axe for WCAG compliance. Use when adding or validating a11y tests, running WCAG checks, or auditing UI accessibility.
When the user wants to optimize pharmaceutical supply chains, manage cold chain logistics, ensure regulatory compliance, or implement serialization. Also use when the user mentions "pharma supply chain," "GMP compliance," "cold chain," "drug serialization," "clinical trials logistics," "pharmaceutical distribution," "good distribution practices," "GDP," "drug safety," or "pharmaceutical quality." For general healthcare, see hospital-logistics. For clinical trials specifically, see clinical-trial-logistics.