@alirezarezvani
CTO in HealthTech | Engineering AI that helps people move safely and live better . Augmented AI | Agentic Coding | Turning complex problems into simple solution
353 skills8 repositories 31.2K
Review Claude Code’s automatically saved memory to identify outdated entries, duplicates, and conflicts with existing instructions.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.
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.
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.
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.
Move browser tests from Cypress or Selenium to Playwright with file-by-file conversion and verification. The skill also adapts shared helpers and element selectors, updates CI workflows and documentation, and reports tests that need manual work.
Prepare internal audit materials for ISO/IEC 42001:2023, the AI management system standard. Identify gaps, link AI risks to controls, and build a 12-month audit plan with coverage priorities and auditor independence checks.
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.
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.
Examine a plan by imagining it has failed twelve months later. Identify weak assumptions, linked dependencies, and commitments that are hard to reverse, then outline validation steps and criteria for continuing, changing direction, or stopping.
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.
Plan ISO 27001 information security audits, review evidence that security controls work, and document findings. The skill also helps classify failures, track corrective actions, and prepare documentation for certification audits.
Examine business assumptions behind revenue forecasts, market estimates, or hiring plans. Identify counter-evidence, model worse outcomes, assess how changes affect results, and propose validation steps, backup plans, and early warning indicators.
Set up Playwright, a browser testing tool, for an existing web project. Generate configuration, test folders, an example test, and applicable CI automation, then run the test and address setup failures.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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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