[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"skill:01M6EK0CDZP9PWSH70C604JM8N":3,"skill-same:01M6EK0CDZP9PWSH70C604JM8N":65},{"skillNo":4,"name":5,"nameZh":6,"description":7,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":6,"repositoryNo":12,"starsCount":13,"licenseSpdxId":14,"licenseFileUrl":6,"sourceHtmlUrl":15,"categories":16,"keywords":22,"publishedAt":27,"linkOnly":28,"markdownContent":29,"markdownBody":30,"frontMatter":31,"refName":32,"commitSha":33,"skillDirectory":34,"forksCount":35,"repositoryHtmlUrl":36,"repositoryHomepageUrl":6,"ownerHtmlUrl":37,"ownerBlogUrl":6,"ownerDescription":6,"updatedAt":38,"install":39,"resources":52},"01M6EK0CDZP9PWSH70C604JM8N","agent-workflow-designer",null,"Agent Workflow Designer","ArogyaReddy\u002Falirezarezvani-claude-skills","ArogyaReddy","https:\u002F\u002Favatars.githubusercontent.com\u002Fu\u002F12032101?v=4","01M6EJA7DAM8950XYAD875F4NY","01M6EJA7JSMD9SN617EJHTF2BQ",39,"MIT","https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fengineering\u002Fagent-workflow-designer\u002FSKILL.md",[17],{"categoryNo":18,"categoryName":19,"taxonomyType":20,"taxonomyTypeDesc":21},"01JBSEEDCAT000000000000023","Skill与智能体开发","SCENARIO","使用场景",[23,24,25,26],"workflow","designer","agent workflow designer","agent workflow","2026-11-10 10:12:30",false,"---\nname: \"agent-workflow-designer\"\ndescription: \"Agent Workflow Designer\"\n---\n\n# Agent Workflow Designer\n\n**Tier:** POWERFUL  \n**Category:** Engineering  \n**Domain:** Multi-Agent Systems \u002F AI Orchestration\n\n---\n\n## Overview\n\nDesign production-grade multi-agent workflows with clear pattern choice, handoff contracts, failure handling, and cost\u002Fcontext controls.\n\n## Core Capabilities\n\n- Workflow pattern selection for multi-step agent systems\n- Skeleton config generation for fast workflow bootstrapping\n- Context and cost discipline across long-running flows\n- Error recovery and retry strategy scaffolding\n- Documentation pointers for operational pattern tradeoffs\n\n---\n\n## When to Use\n\n- A single prompt is insufficient for task complexity\n- You need specialist agents with explicit boundaries\n- You want deterministic workflow structure before implementation\n- You need validation loops for quality or safety gates\n\n---\n\n## Quick Start\n\n```bash\n# Generate a sequential workflow skeleton\npython3 scripts\u002Fworkflow_scaffolder.py sequential --name content-pipeline\n\n# Generate an orchestrator workflow and save it\npython3 scripts\u002Fworkflow_scaffolder.py orchestrator --name incident-triage --output workflows\u002Fincident-triage.json\n```\n\n---\n\n## Pattern Map\n\n- `sequential`: strict step-by-step dependency chain\n- `parallel`: fan-out\u002Ffan-in for independent subtasks\n- `router`: dispatch by intent\u002Ftype with fallback\n- `orchestrator`: planner coordinates specialists with dependencies\n- `evaluator`: generator + quality gate loop\n\nDetailed templates: `references\u002Fworkflow-patterns.md`\n\n---\n\n## Recommended Workflow\n\n1. Select pattern based on dependency shape and risk profile.\n2. Scaffold config via `scripts\u002Fworkflow_scaffolder.py`.\n3. Define handoff contract fields for every edge.\n4. Add retry\u002Ftimeouts and output validation gates.\n5. Dry-run with small context budgets before scaling.\n\n---\n\n## Common Pitfalls\n\n- Over-orchestrating tasks solvable by one well-structured prompt\n- Missing timeout\u002Fretry policies for external-model calls\n- Passing full upstream context instead of targeted artifacts\n- Ignoring per-step cost accumulation\n\n## Best Practices\n\n1. Start with the smallest pattern that can satisfy requirements.\n2. Keep handoff payloads explicit and bounded.\n3. Validate intermediate outputs before fan-in synthesis.\n4. Enforce budget and timeout limits in every step.\n","# Agent Workflow Designer\n\n**Tier:** POWERFUL  \n**Category:** Engineering  \n**Domain:** Multi-Agent Systems \u002F AI Orchestration\n\n---\n\n## Overview\n\nDesign production-grade multi-agent workflows with clear pattern choice, handoff contracts, failure handling, and cost\u002Fcontext controls.\n\n## Core Capabilities\n\n- Workflow pattern selection for multi-step agent systems\n- Skeleton config generation for fast workflow bootstrapping\n- Context and cost discipline across long-running flows\n- Error recovery and retry strategy scaffolding\n- Documentation pointers for operational pattern tradeoffs\n\n---\n\n## When to Use\n\n- A single prompt is insufficient for task complexity\n- You need specialist agents with explicit boundaries\n- You want deterministic workflow structure before implementation\n- You need validation loops for quality or safety gates\n\n---\n\n## Quick Start\n\n```bash\n# Generate a sequential workflow skeleton\npython3 scripts\u002Fworkflow_scaffolder.py sequential --name content-pipeline\n\n# Generate an orchestrator workflow and save it\npython3 scripts\u002Fworkflow_scaffolder.py orchestrator --name incident-triage --output workflows\u002Fincident-triage.json\n```\n\n---\n\n## Pattern Map\n\n- `sequential`: strict step-by-step dependency chain\n- `parallel`: fan-out\u002Ffan-in for independent subtasks\n- `router`: dispatch by intent\u002Ftype with fallback\n- `orchestrator`: planner coordinates specialists with dependencies\n- `evaluator`: generator + quality gate loop\n\nDetailed templates: `references\u002Fworkflow-patterns.md`\n\n---\n\n## Recommended Workflow\n\n1. Select pattern based on dependency shape and risk profile.\n2. Scaffold config via `scripts\u002Fworkflow_scaffolder.py`.\n3. Define handoff contract fields for every edge.\n4. Add retry\u002Ftimeouts and output validation gates.\n5. Dry-run with small context budgets before scaling.\n\n---\n\n## Common Pitfalls\n\n- Over-orchestrating tasks solvable by one well-structured prompt\n- Missing timeout\u002Fretry policies for external-model calls\n- Passing full upstream context instead of targeted artifacts\n- Ignoring per-step cost accumulation\n\n## Best Practices\n\n1. Start with the smallest pattern that can satisfy requirements.\n2. Keep handoff payloads explicit and bounded.\n3. Validate intermediate outputs before fan-in synthesis.\n4. Enforce budget and timeout limits in every step.\n",{"name":5,"description":7},"main","dc799ac68cfdc454fc55edaf3f054651f645f738","engineering\u002Fagent-workflow-designer",10,"https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills","https:\u002F\u002Fgithub.com\u002FArogyaReddy","2026-03-18 00:40:19",{"source":8,"skillName":5,"commands":40,"prompt":50,"zipAvailable":51},[41,44,47],{"tool":42,"command":43},"npx","npx skills add ArogyaReddy\u002Falirezarezvani-claude-skills --skill agent-workflow-designer",{"tool":45,"command":46},"bunx","bunx skills add ArogyaReddy\u002Falirezarezvani-claude-skills --skill agent-workflow-designer",{"tool":48,"command":49},"pnpm","pnpm dlx skills add ArogyaReddy\u002Falirezarezvani-claude-skills --skill agent-workflow-designer","安装技能，技能地址：https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fengineering\u002Fagent-workflow-designer\u002FSKILL.md",true,[53,59],{"path":54,"resourceType":55,"resourceTypeDesc":56,"sizeBytes":57,"sourceHtmlUrl":58},"references\u002Fworkflow-patterns.md","REFERENCE","参考文档",1518,"https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fengineering\u002Fagent-workflow-designer\u002Freferences\u002Fworkflow-patterns.md",{"path":60,"resourceType":61,"resourceTypeDesc":62,"sizeBytes":63,"sourceHtmlUrl":64},"scripts\u002Fworkflow_scaffolder.py","SCRIPT","脚本",3365,"https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fengineering\u002Fagent-workflow-designer\u002Fscripts\u002Fworkflow_scaffolder.py",[66,93,119,149,169,192],{"skillNo":67,"name":68,"nameZh":6,"description":69,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":6,"repositoryNo":12,"starsCount":13,"licenseSpdxId":14,"licenseFileUrl":6,"sourceHtmlUrl":70,"categories":71,"keywords":72,"publishedAt":27},"01M6EKFK0DB8WVYWCN59CM5SEQ","risk-management-specialist","Medical device risk management specialist implementing ISO 14971 throughout product lifecycle. Provides risk analysis, risk evaluation, risk control, and post-production information analysis. Use when user mentions risk management, ISO 14971, risk analysis, FMEA, fault tree analysis, hazard identification, risk control, risk matrix, benefit-risk analysis, residual risk, risk acceptability, or post-market risk.","https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fra-qm-team\u002Frisk-management-specialist\u002FSKILL.md",[],[73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92],"risk","risk management specialist","management","risk management","risk analysis","risk evaluation","product","Evaluation","Production","lifecycle","analysis","use","risk matrix","Market","control","iso","medical","iso 14971","identification","post",{"skillNo":94,"name":95,"nameZh":6,"description":96,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":6,"repositoryNo":12,"starsCount":13,"licenseSpdxId":14,"licenseFileUrl":6,"sourceHtmlUrl":97,"categories":98,"keywords":99,"publishedAt":27},"01M6EKFDZ7KES3X3HH8KBHR9JF","regulatory-affairs-head","Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathways for new medical devices; drafts responses to FDA deficiency letters and Notified Body queries; develops CE marking technical documentation under EU MDR 2017\u002F745; coordinates multi-market approval strategies across FDA, EU, Health Canada, PMDA, and NMPA; and maintains regulatory intelligence on evolving standards. Use when users need to plan or execute FDA submissions, navigate 510(k) or PMA approval processes, achieve CE marking, prepare pre-submission meeting materials, write regulatory strategy documents, respond to agency queries, or manage compliance documentation for medical device market access.","https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fra-qm-team\u002Fregulatory-affairs-head\u002FSKILL.md",[],[100,101,102,103,104,105,106,107,108,109,110,111,112,113,89,114,115,116,117,118],"regulatory affairs head","regulatory","head","documentation","documents","packages","plan","access","write","evidence","standards","intelligence","across","strategies","clinical","pathway","de","respond","medical devices",{"skillNo":120,"name":121,"nameZh":6,"description":122,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":6,"repositoryNo":12,"starsCount":13,"licenseSpdxId":14,"licenseFileUrl":6,"sourceHtmlUrl":123,"categories":124,"keywords":133,"publishedAt":27},"01M6EKF980P5MQBEQQAKB2JE6V","quality-manager-qms-iso13485","ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support. Use when working with medical device quality systems, preparing for ISO 13485 audits, managing regulatory compliance documentation, setting up corrective actions, or building audit preparation programs. Useful for quality management, audit preparation, regulatory compliance, medical device documentation, and corrective action workflows.","https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fra-qm-team\u002Fquality-manager-qms-iso13485\u002FSKILL.md",[125,128],{"categoryNo":126,"categoryName":127,"taxonomyType":20,"taxonomyTypeDesc":21},"01JBSEEDCAT000000000000015","视觉设计",{"categoryNo":129,"categoryName":130,"taxonomyType":131,"taxonomyTypeDesc":132},"01JBSEEDCAT000000000000032","设计师","PROFESSION","适用职业",[134,135,136,137,138,139,103,140,141,142,143,84,144,145,146,87,88,89,147,148],"quality manager qms iso13485","quality","design","review","support","workflows","audit","actions","compliance","system","up","maintenance","document","records","ISO 13485",{"skillNo":150,"name":151,"nameZh":6,"description":152,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":6,"repositoryNo":12,"starsCount":13,"licenseSpdxId":14,"licenseFileUrl":6,"sourceHtmlUrl":153,"categories":154,"keywords":158,"publishedAt":27},"01M6EKF4ZN8ZJJP3K6FM1WEM85","quality-manager-qmr","Senior Quality Manager Responsible Person (QMR) for HealthTech and MedTech companies. Provides quality system governance, management review leadership, regulatory compliance oversight, and quality performance monitoring per ISO 13485 Clause 5.5.2.","https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fra-qm-team\u002Fquality-manager-qmr\u002FSKILL.md",[155],{"categoryNo":156,"categoryName":157,"taxonomyType":131,"taxonomyTypeDesc":132},"01JBSEEDCAT000000000000037","律师与法务",[159,135,137,160,161,162,163,142,164,143,75,165,101,166,167,168,88,148],"quality manager qmr","policy","performance","governance","monitoring","regulatory compliance","oversight","cost","culture","leadership",{"skillNo":170,"name":171,"nameZh":6,"description":172,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":6,"repositoryNo":12,"starsCount":13,"licenseSpdxId":14,"licenseFileUrl":6,"sourceHtmlUrl":173,"categories":174,"keywords":179,"publishedAt":27},"01M6EKF15YKH2AQB45MH4Y6S08","quality-documentation-manager","Document control system management for medical device QMS. Covers document numbering, version control, change management, and 21 CFR Part 11 compliance. Use for document control procedures, change control workflow, document numbering, version management, electronic signature compliance, or regulatory documentation review.","https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fra-qm-team\u002Fquality-documentation-manager\u002FSKILL.md",[175,178],{"categoryNo":176,"categoryName":177,"taxonomyType":20,"taxonomyTypeDesc":21},"01JBSEEDCAT000000000000002","文档处理",{"categoryNo":156,"categoryName":157,"taxonomyType":131,"taxonomyTypeDesc":132},[103,180,135,137,23,181,140,82,182,143,183,184,185,186,187,89,188,189,190,191],"quality documentation manager","change","document lifecycle","change management","list","master","system management","documentation review","cfr","21 cfr part 11","change control","retention",{"skillNo":193,"name":194,"nameZh":6,"description":195,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":6,"repositoryNo":12,"starsCount":13,"licenseSpdxId":14,"licenseFileUrl":6,"sourceHtmlUrl":196,"categories":197,"keywords":198,"publishedAt":27},"01M6EKEXQMCQC11A5WR9GEPC4S","qms-audit-expert","ISO 13485 internal audit expertise for medical device QMS. Covers audit planning, execution, nonconformity classification, and CAPA verification. Use for internal audit planning, audit execution, finding classification, external audit preparation, or audit program management.","https:\u002F\u002Fgithub.com\u002FArogyaReddy\u002Falirezarezvani-claude-skills\u002Fblob\u002Fmain\u002Fra-qm-team\u002Fqms-audit-expert\u002FSKILL.md",[],[140,199,200,201,202,203,204,205,75,84,206,207,88,89,148],"qms audit expert","expert","planning","verification","execution","classification","schedule","checklist","device"]