Agent Skills Directory
Browse production-ready skills for Claude Code, Cursor, Codex, Gemini CLI, and more. Install in seconds to supercharge your AI coding assistant.
Change Request
Create a change management request with impact analysis and rollback plan. Use when proposing a system or process change that needs approval, preparing a change record for CAB review, documenting risk and rollback steps before a deployment, or planning stakeholder communications for a rollout.
Capacity Plan
Plan resource capacity — workload analysis and utilization forecasting. Use when heading into quarterly planning, the team feels overallocated and you need the numbers, deciding whether to hire or deprioritize, or stress-testing whether upcoming projects fit the people you have.
Resume
Resume a paused experiment. Checkout the experiment branch, read results history, continue iterating.
Testrail
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Status
Memory health dashboard showing line counts, topic files, capacity, stale entries, and recommendations.
Documentation
Write and maintain technical documentation. Trigger with "write docs for", "document this", "create a README", "write a runbook", "onboarding guide", or when the user needs help with any form of technical writing — API docs, architecture docs, or operational runbooks.
Debug
Structured debugging session — reproduce, isolate, diagnose, and fix. Trigger with an error message or stack trace, "this works in staging but not prod", "something broke after the deploy", or when behavior diverges from expected and the cause isn't obvious.
Database Designer
Database Designer - POWERFUL Tier Skill
Status Report
Generate a status report with KPIs, risks, and action items. Use when writing a weekly or monthly update for leadership, summarizing project health with green/yellow/red status, surfacing risks and decisions that need stakeholder attention, or turning a pile of project tracker activity into a readable narrative.
Git Worktree Manager
Git Worktree Manager
Observability Designer
Observability Designer (POWERFUL)
MDR 745 Specialist
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, and EUDAMED integration.