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Found 969 Skills
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.
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.
3-gate regulatory template orchestrator - manages setup, Gate 1 (analysis), Gate 2 (validation), Gate 3 (generation) for BACEN/RFB compliance.
This skill should be used when the user asks to "test the triage skill", "run triage tests", "validate antithesis triage", "test:triage", or "smoke test triage". Orchestrates end-to-end testing of the antithesis-triage skill by running real triage operations via sub-agents and reviewing the results for bugs, skill compliance issues, and papercuts.
HarmonyOS code review skill for auditing ArkTS projects against official Huawei development guidelines and security best practices. Use when reviewing HarmonyOS applications for: (1) Security compliance (hardcoded credentials, encryption, input validation), (2) ArkTS language standards (hilog usage, type safety, magic numbers), (3) Component lifecycle management (resource cleanup, event subscription handling), (4) State management (V1/V2 decorator consistency), (5) Database operations (ResultSet handling, transaction management, encryption), (6) Permission management (official permission patterns), (7) Performance issues (async forEach, resource leaks), (8) API version compatibility, (9) Kit usage best practices. Generates comprehensive markdown reports with prioritized fix recommendations.
Interactive skill creation and import with automated validation and marketplace compliance. Use when: - "Create a new skill" - "Import an existing skill" - "Create a new agentic pack" - "Add skill to <pack>" - "Build skill for <rh-product>" - User mentions "skill builder", "contribute", "new skill", "import skill", or "new pack" Two modes: create from scratch or import existing SKILL.md. Guides through discovery, definition, generation, and validation. Enforces SKILL_DESIGN_PRINCIPLES.md and agentskills.io spec.
When the user wants to find, qualify, and build a list of prospects to reach out to — across B2B SaaS, general B2B, or local small businesses. Also use when the user mentions "prospecting," "build a prospect list," "find prospects," "find leads," "lead gen list," "find SaaS companies that," "find B2B companies," "find local businesses," "ICP-fit accounts," "who should we go after," "outbound list," "target account list," "find clients near me," "businesses without websites," "prospect research," or "qualified leads." Use this for the list-building and qualification phase. For writing the outbound copy after the list is built, see cold-email. For deep competitive research on specific accounts, see competitor-profiling.
Validate that a branch or pull request implementation matches introduced product, technical, security, and related specs. Use when reviewing or finishing a spec-driven change and resolving mismatches between checked-in specs and implementation.
Comprehensive toolkit for preparing ISO 13485 certification documentation for medical device Quality Management Systems. Use when users need help with ISO 13485 QMS documentation, including (1) conducting gap analysis of existing documentation, (2) creating Quality Manuals, (3) developing required procedures and work instructions, (4) preparing Medical Device Files, (5) understanding ISO 13485 requirements, or (6) identifying missing documentation for medical device certification. Also use when users mention medical device regulations, QMS certification, FDA QMSR, EU MDR, or need help with quality system documentation.
Initialize and manage the evidence collection directory for professional security audits with documented proof of findings.
Derive security requirements from threat models and business context. Use when translating threats into actionable requirements, creating security user stories, or building security test cases.