Alireza Rezvani

Summarize Playwright test results in a Markdown report with failures, timings, and tests that pass only after retries. Use configured reporting destinations and compare earlier reports when historical results are available.

中文简介正在准备中。当前显示英语简介。

• Summarizing the latest Playwright test run
• Reviewing failed tests and their error messages
• Sharing results through configured Slack or TestRail connections

Build and maintain a medical device quality management system using ISO 13485:2016 workflows. It supports gap analysis, controlled documentation, internal audits, corrective and preventive actions, process validation, and supplier evaluation, with templates and an audit checklist generator.

中文简介正在准备中。当前显示英语简介。

• Planning a medical device quality management system
• Standardizing document approval and revision control
• Preparing internal audits and certification reviews

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.

中文简介正在准备中。当前显示英语简介。

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

Review Claude Code’s automatically saved memory to identify outdated entries, duplicates, and conflicts with existing instructions.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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• Reviewing lessons saved after a major development task
• Finding outdated or conflicting memory entries
• Identifying recurring lessons to turn into rules

Prepare SaaS teams for SOC 2 audits by mapping evaluation criteria to controls, the measures used to manage risk. Build control matrices, track supporting evidence, identify gaps, and assess readiness for Type I or Type II.

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• Build a matrix of controls, owners, and evidence requirements
• Identify gaps in Type I or Type II audit preparation
• Track evidence collection for each control

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

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

Turn recurring lessons in Claude's automatic memory into concise project rules. Choose a project-wide, file-specific, or personal rule location, include concrete commands, and clean up the original memory entry after confirmation.

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• Make repeated corrections into lasting rules
• Record the project's package manager
• Apply API rules to selected file paths

Help quality leaders at medical technology companies prepare management reviews, define quality objectives, and track performance indicators. Organize audit findings, complaints, corrective actions, and regulatory status into reports and assigned improvement actions.

中文简介正在准备中。当前显示英语简介。

• Preparing quality management reviews
• Defining measurable quality objectives and indicators
• Tracking audit findings and corrective actions

Review code for privacy risks, prepare data protection impact assessments, and track personal data requests and deadlines. The skill supports GDPR and German privacy compliance work, with final compliance decisions referred to a data protection officer or legal counsel.

中文简介正在准备中。当前显示英语简介。

• Checking a service's code for privacy risks
• Preparing a data protection impact assessment
• Tracking deadlines for access and erasure requests

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

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。

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

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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• 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

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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• 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.

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

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

Support information security management for healthcare and medical technology companies. Structure an ISO 27001 management system, assess risks, review security controls, and prepare audit evidence, gap reports, and incident response procedures.

中文简介正在准备中。当前显示英语简介。

• Planning an information security management system
• Assessing risks to patient data and medical devices
• Finding gaps in security control implementation

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

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.

中文简介正在准备中。当前显示英语简介。

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

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

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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• 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.

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• 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

Work through difficult business decisions such as layoffs, product closures, or changes in company direction. Compare immediate and long-term consequences, map who is affected, and prepare a clear explanation and communication plan.

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• Weighing layoffs and their impact on the team
• Comparing options for closing a product line
• Considering a co-founder's role change or departure

Automate Google Workspace tasks with the gws command-line tool, including email, file management, spreadsheets, and scheduling. Get guidance on installation, authentication, reusable workflow templates, and security audits of sharing and account settings.

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• Automating Gmail sending and inbox organization
• Managing Drive files and sharing permissions
• Reading and updating Sheets data