Turns recurring workflows and proven debugging solutions into reusable skill packages. It creates SKILL.md, a readable overview, and optional supporting examples from a user description or saved project memory, with checks for completeness and portability.
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Explicitly save debugging discoveries, project conventions, and working preferences to Claude's persistent project memory. The skill checks for duplicate notes, keeps entries concise, and suggests moving enforceable rules into CLAUDE.md when appropriate.
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Build market research evidence by comparing two market-size estimates, calculating survey sample sizes for each customer group, and scoring potential segments. Outputs show methods and assumptions so teams can assess the basis for business decisions.
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Connect TestRail test cases with Playwright automated tests. Generate tests from documented steps, send execution results back, create test runs, and check which cases remain unlinked using case IDs recorded in each test.
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Challenge business plans, prepare for difficult board questions, and work through decisions with painful tradeoffs. This skill identifies assumptions and failure risks, examines stakeholder impacts, and turns postmortems into changes with clear owners and verification dates.
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Review Playwright browser tests against 20 quality checks to find unreliable patterns and missing coverage. Get scores for each file, prioritized findings, and corrected code for critical issues.
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Organize document control for medical device quality management, including numbering, revisions, approvals, and change workflows. Includes guidance on electronic records and signatures, plus a Python validator for document metadata and completeness checks.
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Plan a prospective clinical study by ranking endpoints, estimating participant numbers and statistical power, and assessing feasibility. Outputs include assumptions and named reviewers, providing material for expert review before a protocol is finalized.
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Plan R&D budgets with direct and indirect costs, track spending and how long funds will last, and check whether milestones remain affordable. Prepare accounting review routes for development costs, with explicit assumptions and a named finance owner.
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Compare application pages, interactive components, API endpoints, and key user journeys with existing tests. Get a coverage matrix, an estimated coverage percentage, and a prioritized plan for missing tests with suggested templates and effort estimates.
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Route enterprise research questions to specialized skills for clinical studies, R&D finance, market research, or user research. Receive a concise digest of findings, next actions, output files, and assumptions that need human review.
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Supports medical device risk management from planning through post-market review using ISO 14971:2019. Helps identify hazards, evaluate risks, select and verify controls, assess remaining risks, and maintain records as new information arrives.
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Organize EU AI Act compliance work with references to Articles and Annexes. Classify AI systems by risk, plan conformity assessments that check regulatory requirements, prepare technical documentation checklists, and map obligations and deadlines to organizational roles.
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Review Claude Code’s automatically saved memory to identify outdated entries, duplicates, and conflicts with existing instructions. Produces a health report and recommendations for consolidating notes or turning recurring lessons into lasting project rules.
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Check the state of an agent’s project memory with a dashboard of line counts, topic files, capacity, outdated file references, and duplicates. Get cleanup recommendations or request a one-line status summary.
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Plan and conduct internal audits for medical device quality management systems under ISO 13485. Organize evidence, classify findings, verify corrective and preventive actions, and prepare for external audits with structured checklists and risk-based scheduling.
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Analyze failed launches, missed targets, or unsuccessful hires through a blameless review. Use five successive why questions to identify root causes, then record concrete changes with owners, deadlines, and ways to verify results.
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Supports preparation for EU medical device regulation reviews by organizing device classification, technical documentation, clinical evidence, and post-market monitoring. Includes a tool to identify documentation and compliance gaps and prioritize the next steps.
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Run Playwright tests on BrowserStack to check behavior across browsers and devices. Configure cloud connections, compare results by browser, inspect session videos and logs, and set up a tunnel for testing local or restricted environments.
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Prepare medical device regulatory strategies and submission documents for FDA, EU, and other markets. Compare application routes, organize technical and clinical evidence, draft responses to regulator questions, and track submission schedules.
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Supports medical device quality investigations through CAPA, a process for corrective and preventive action. Helps identify root causes, plan actions, verify results, and report overdue cases, recurrence rates, and other program metrics.
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Audit web applications for accessibility issues against WCAG 2.2 Level A and AA, the web accessibility standards. Get framework-specific code fixes, contrast checks, verification steps, and reports, with options for automated checks in development pipelines.
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Prepare medical device regulatory work for the US FDA. Compare submission routes, organize required documents, review quality management requirements, assess patient data safeguards under HIPAA, and plan device cybersecurity documentation and controls.
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Set up Playwright browser tests, generate cases from specifications or URLs, and review coverage gaps. Diagnose tests that fail inconsistently, migrate Cypress or Selenium suites, and optionally connect TestRail and BrowserStack for results and browser testing.
中文简介正在准备中。当前显示英语简介。