alirezarezvani

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Saving a debugging solution as a reusable skill
• Packaging recurring workflows for other projects
• Turning saved project knowledge into documented procedures

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Preserving hard-won debugging discoveries
• Recording undocumented project conventions
• Remembering tool-specific commands and pitfalls

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Estimating market size for a business decision
• Planning survey responses for each customer segment
• Evaluating which market segments to pursue

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Generating Playwright tests from TestRail cases
• Sending automated test results to TestRail
• Creating a test run for regression testing

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Find weaknesses in a business plan
• Prepare answers to difficult board questions
• Compare options for a difficult management decision

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Reviewing a specific Playwright test file
• Auditing test quality across a project
• Finding causes of unreliable test runs

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Defining document numbering and revision rules
• Designing review and approval workflows
• Organizing document changes and impact assessments

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Choosing primary and secondary study endpoints
• Estimating sample size with dropout allowance
• Assessing feasibility before a study review

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Build an R&D budget with an explicit indirect-cost split
• Check whether remaining funds cover the next milestone
• Prepare development costs for accounting review

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Finding untested pages, components, and API endpoints
• Prioritizing tests for sign-in, payments, and core features
• Planning test counts, templates, and effort for coverage gaps

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Plan a clinical study and sample size
• Review R&D budgets and spending classifications
• Estimate market size and design surveys

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Create a medical device risk management plan
• Identify hazards and choose risk analysis methods
• Compare risk controls and assess remaining risks

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Reviewing risk classification for a new AI system
• Planning conformity assessments for high-risk AI
• Preparing technical documentation checklists

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Reviewing lessons saved after a major development task
• Finding outdated or conflicting memory entries
• Identifying recurring lessons to turn into rules

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Checking how full project memory is
• Finding references to deleted files
• Reviewing memory and rule file sizes

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Plan an annual internal audit schedule
• Document audit evidence and classify findings
• Verify the effectiveness of corrective actions

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Investigating why a release was delayed
• Reviewing a missed sales or revenue target
• Examining a hiring decision that did not work out

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Documenting a device classification rationale under MDR
• Checking technical documentation before a review
• Planning clinical evaluation and identifying evidence gaps

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Checking browser compatibility with Playwright tests
• Configuring BrowserStack cloud test connections
• Investigating failures through session videos and logs

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Comparing FDA application routes for a new medical device
• Organizing technical documentation for EU MDR
• Drafting responses to FDA or Notified Body questions

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Investigating recurring quality problems
• Planning corrective actions after audit findings
• Checking whether corrective actions prevented recurrence

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Audit a web application before release
• Fix contrast and keyboard navigation issues
• Prepare accessibility reports for stakeholders

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Compare 510(k), PMA, and De Novo submission routes
• Organize required 510(k) documents and submission milestones
• Review quality documentation against QMSR and ISO 13485:2016

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.

한국어 요약은 준비 중입니다. 영어 요약을 표시하고 있습니다.

• Set up Playwright tests and CI
• Generate and review tests from user stories
• Diagnose tests that fail inconsistently