[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"skill:01M6AF2V6TYEZDMHQV1BF14P1S":3,"skill-same:01M6AF2V6TYEZDMHQV1BF14P1S":91},{"skillNo":4,"name":5,"nameZh":6,"description":7,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":16,"categories":17,"keywords":23,"publishedAt":44,"linkOnly":45,"markdownContent":46,"markdownBody":47,"frontMatter":48,"refName":49,"commitSha":50,"skillDirectory":51,"forksCount":52,"repositoryHtmlUrl":53,"repositoryHomepageUrl":54,"ownerHtmlUrl":55,"ownerBlogUrl":56,"ownerDescription":57,"updatedAt":58,"install":59,"resources":72},"01M6AF2V6TYEZDMHQV1BF14P1S","quality-manager-qms-iso13485",null,"ISO 13485 Quality Management System specialist for medical device companies. Provides QMS implementation, maintenance, process optimization, and compliance expertise. Use for QMS design, documentation control, management review, internal auditing, corrective actions, and ISO 13485 certification activities.","davila7\u002Fclaude-code-templates","davila7","https:\u002F\u002Favatars.githubusercontent.com\u002Fu\u002F6216945?v=4","01M6ADEWWFPS191NFM0Y1EX1JH","Daniel Avila","01M6ADJHGM78PHQRD3XZTFDVKK",33481,"MIT","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-manager-qms-iso13485\u002FSKILL.md",[18],{"categoryNo":19,"categoryName":20,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000015","视觉设计","SCENARIO","使用场景",[24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43],"manager","quality manager qms iso13485","quality","maintenance","expertise","for","quality management system","ISO 13485","medical","iso","iso 13485 certification","control","design","use","system","Optimization","compliance","actions","documentation","review","2026-11-10 10:12:30",false,"---\nname: quality-manager-qms-iso13485\ndescription: ISO 13485 Quality Management System specialist for medical device companies. Provides QMS implementation, maintenance, process optimization, and compliance expertise. Use for QMS design, documentation control, management review, internal auditing, corrective actions, and ISO 13485 certification activities.\n---\n\n# Senior Quality Manager - QMS ISO 13485 Specialist\n\nExpert-level ISO 13485 Quality Management System implementation and maintenance for medical device organizations with deep knowledge of quality processes, documentation control, and continuous improvement.\n\n## Core QMS Competencies\n\n### 1. ISO 13485 QMS Implementation\nDesign and implement comprehensive quality management systems aligned with ISO 13485:2016 and regulatory requirements.\n\n**Implementation Workflow:**\n1. **Gap Analysis and Planning**\n   - Current state assessment against ISO 13485 requirements\n   - Gap identification and prioritization\n   - Implementation roadmap development\n   - Resource allocation and timeline planning\n\n2. **QMS Design and Documentation**\n   - **Quality Manual** development per ISO 13485 clause 4.2.2\n   - **Process documentation** creation and mapping\n   - **Procedure development** following references\u002Fiso13485-procedures.md\n   - **Work instruction** standardization\n\n3. **Process Implementation**\n   - Cross-functional training and competency development\n   - Process deployment and monitoring\n   - Performance metrics establishment\n   - Feedback loop integration\n\n### 2. Document Control System (ISO 13485 Clause 4.2.3)\nEstablish and maintain robust document control processes ensuring compliance and traceability.\n\n**Document Control Framework:**\n```\nDOCUMENT LIFECYCLE MANAGEMENT\n├── Document Creation and Approval\n│   ├── Template standardization\n│   ├── Review and approval workflow\n│   ├── Version control system\n│   └── Release authorization\n├── Document Distribution and Access\n│   ├── Controlled distribution matrix\n│   ├── Access permission management\n│   ├── Electronic system integration\n│   └── External document control\n├── Document Maintenance and Updates\n│   ├── Periodic review scheduling\n│   ├── Change control procedures\n│   ├── Impact assessment process\n│   └── Superseded document management\n└── Document Retention and Disposal\n    ├── Retention period definition\n    ├── Archive management system\n    ├── Disposal authorization\n    └── Legal\u002Fregulatory compliance\n```\n\n### 3. Management Review Process (ISO 13485 Clause 5.6)\nFacilitate effective management review meetings ensuring systematic QMS evaluation and improvement.\n\n**Management Review Structure:**\n- **Quarterly Management Review** meetings with senior leadership\n- **Input preparation** covering all ISO 13485 clause 5.6.2 requirements\n- **Decision tracking** and action item management\n- **Follow-up verification** and effectiveness monitoring\n\n**Key Review Inputs:**\n- Audit results (internal and external)\n- Customer feedback and complaints\n- Process performance and product conformity\n- Corrective and preventive actions status\n- Changes affecting the QMS\n- Improvement recommendations\n\n### 4. Internal Audit Program (ISO 13485 Clause 8.2.2)\nDesign and execute comprehensive internal audit programs ensuring QMS effectiveness and continuous improvement.\n\n**Audit Program Management:**\n1. **Annual Audit Planning**\n   - Risk-based audit scheduling\n   - Competent auditor assignment\n   - Scope definition and criteria establishment\n   - **Decision Point**: Determine audit frequency based on process criticality\n\n2. **Audit Execution**\n   - **For Process Audits**: Follow scripts\u002Faudit-checklists\u002Fprocess-audit.py\n   - **For System Audits**: Follow scripts\u002Faudit-checklists\u002Fsystem-audit.py\n   - **For Product Audits**: Follow scripts\u002Faudit-checklists\u002Fproduct-audit.py\n\n3. **Audit Follow-up**\n   - Nonconformity management and CAPA initiation\n   - Corrective action verification\n   - Effectiveness assessment\n   - Audit report completion and distribution\n\n## QMS Process Optimization\n\n### Design Controls (ISO 13485 Clause 7.3)\nImplement robust design controls ensuring systematic product development and risk management integration.\n\n**Design Control Stages:**\n1. **Design Planning** (7.3.2)\n2. **Design Inputs** (7.3.3)\n3. **Design Outputs** (7.3.4)\n4. **Design Review** (7.3.5)\n5. **Design Verification** (7.3.6)\n6. **Design Validation** (7.3.7)\n7. **Design Transfer** (7.3.8)\n8. **Design Changes** (7.3.9)\n\n### Risk Management Integration (ISO 14971)\nEnsure seamless integration of risk management processes throughout the QMS and product lifecycle.\n\n**Risk Management Workflow:**\n- Risk management planning and file establishment\n- Risk analysis and risk evaluation\n- Risk control implementation and verification\n- Production and post-production information analysis\n- Risk management file maintenance\n\n### Supplier Quality Management (ISO 13485 Clause 7.4)\nEstablish comprehensive supplier evaluation, selection, and monitoring processes.\n\n**Supplier Management Process:**\n- Supplier qualification and approval criteria\n- Performance monitoring and evaluation\n- Supplier audit programs\n- Supplier corrective action management\n- Supply chain risk assessment\n\n## QMS Performance Monitoring\n\n### Key Quality Indicators (KQIs)\nMonitor these critical quality metrics:\n- **QMS Process Performance**: Process cycle times, efficiency metrics\n- **Customer Satisfaction**: Complaint trends, satisfaction surveys\n- **Internal Audit Effectiveness**: Finding trends, closure rates\n- **CAPA Performance**: Closure timelines, effectiveness measures\n- **Training Effectiveness**: Competency assessments, compliance rates\n\n### Continuous Improvement\n**Improvement Methodology:**\n1. **Data Collection and Analysis**\n2. **Root Cause Analysis** using references\u002Froot-cause-analysis-tools.md\n3. **Improvement Planning** and resource allocation\n4. **Implementation and Monitoring**\n5. **Effectiveness Verification** and standardization\n\n## Regulatory Interface Management\n\n### ISO 13485 Certification Maintenance\n- Annual surveillance audit preparation\n- Certification body relationship management\n- Nonconformity resolution and follow-up\n- Certificate maintenance and renewal planning\n\n### QMS Integration with Regulatory Requirements\n- MDR Article 10 (Quality Management System) compliance\n- FDA 21 CFR 820 (Quality System Regulation) alignment\n- Other regulatory QMS requirements integration\n- Regulatory inspection readiness\n\n## Resources\n\n### scripts\u002F\n- `qms-performance-dashboard.py`: Automated QMS metrics tracking and reporting\n- `document-control-audit.py`: Document control compliance verification\n- `management-review-prep.py`: Management review input compilation automation\n- `audit-checklists\u002F`: Comprehensive internal audit checklist generators\n\n### references\u002F\n- `iso13485-procedures.md`: Standard operating procedures templates\n- `design-control-templates.md`: Design control documentation templates\n- `risk-management-integration.md`: ISO 14971 integration guidelines\n- `supplier-qualification-criteria.md`: Supplier assessment frameworks\n- `root-cause-analysis-tools.md`: Problem-solving methodologies\n\n### assets\u002F\n- `qms-templates\u002F`: Quality manual, procedure, and work instruction templates\n- `audit-forms\u002F`: Internal audit report and checklist templates\n- `training-materials\u002F`: ISO 13485 training presentations and materials\n- `process-flowcharts\u002F`: Visual process documentation templates\n","# Senior Quality Manager - QMS ISO 13485 Specialist\n\nExpert-level ISO 13485 Quality Management System implementation and maintenance for medical device organizations with deep knowledge of quality processes, documentation control, and continuous improvement.\n\n## Core QMS Competencies\n\n### 1. ISO 13485 QMS Implementation\nDesign and implement comprehensive quality management systems aligned with ISO 13485:2016 and regulatory requirements.\n\n**Implementation Workflow:**\n1. **Gap Analysis and Planning**\n   - Current state assessment against ISO 13485 requirements\n   - Gap identification and prioritization\n   - Implementation roadmap development\n   - Resource allocation and timeline planning\n\n2. **QMS Design and Documentation**\n   - **Quality Manual** development per ISO 13485 clause 4.2.2\n   - **Process documentation** creation and mapping\n   - **Procedure development** following references\u002Fiso13485-procedures.md\n   - **Work instruction** standardization\n\n3. **Process Implementation**\n   - Cross-functional training and competency development\n   - Process deployment and monitoring\n   - Performance metrics establishment\n   - Feedback loop integration\n\n### 2. Document Control System (ISO 13485 Clause 4.2.3)\nEstablish and maintain robust document control processes ensuring compliance and traceability.\n\n**Document Control Framework:**\n```\nDOCUMENT LIFECYCLE MANAGEMENT\n├── Document Creation and Approval\n│   ├── Template standardization\n│   ├── Review and approval workflow\n│   ├── Version control system\n│   └── Release authorization\n├── Document Distribution and Access\n│   ├── Controlled distribution matrix\n│   ├── Access permission management\n│   ├── Electronic system integration\n│   └── External document control\n├── Document Maintenance and Updates\n│   ├── Periodic review scheduling\n│   ├── Change control procedures\n│   ├── Impact assessment process\n│   └── Superseded document management\n└── Document Retention and Disposal\n    ├── Retention period definition\n    ├── Archive management system\n    ├── Disposal authorization\n    └── Legal\u002Fregulatory compliance\n```\n\n### 3. Management Review Process (ISO 13485 Clause 5.6)\nFacilitate effective management review meetings ensuring systematic QMS evaluation and improvement.\n\n**Management Review Structure:**\n- **Quarterly Management Review** meetings with senior leadership\n- **Input preparation** covering all ISO 13485 clause 5.6.2 requirements\n- **Decision tracking** and action item management\n- **Follow-up verification** and effectiveness monitoring\n\n**Key Review Inputs:**\n- Audit results (internal and external)\n- Customer feedback and complaints\n- Process performance and product conformity\n- Corrective and preventive actions status\n- Changes affecting the QMS\n- Improvement recommendations\n\n### 4. Internal Audit Program (ISO 13485 Clause 8.2.2)\nDesign and execute comprehensive internal audit programs ensuring QMS effectiveness and continuous improvement.\n\n**Audit Program Management:**\n1. **Annual Audit Planning**\n   - Risk-based audit scheduling\n   - Competent auditor assignment\n   - Scope definition and criteria establishment\n   - **Decision Point**: Determine audit frequency based on process criticality\n\n2. **Audit Execution**\n   - **For Process Audits**: Follow scripts\u002Faudit-checklists\u002Fprocess-audit.py\n   - **For System Audits**: Follow scripts\u002Faudit-checklists\u002Fsystem-audit.py\n   - **For Product Audits**: Follow scripts\u002Faudit-checklists\u002Fproduct-audit.py\n\n3. **Audit Follow-up**\n   - Nonconformity management and CAPA initiation\n   - Corrective action verification\n   - Effectiveness assessment\n   - Audit report completion and distribution\n\n## QMS Process Optimization\n\n### Design Controls (ISO 13485 Clause 7.3)\nImplement robust design controls ensuring systematic product development and risk management integration.\n\n**Design Control Stages:**\n1. **Design Planning** (7.3.2)\n2. **Design Inputs** (7.3.3)\n3. **Design Outputs** (7.3.4)\n4. **Design Review** (7.3.5)\n5. **Design Verification** (7.3.6)\n6. **Design Validation** (7.3.7)\n7. **Design Transfer** (7.3.8)\n8. **Design Changes** (7.3.9)\n\n### Risk Management Integration (ISO 14971)\nEnsure seamless integration of risk management processes throughout the QMS and product lifecycle.\n\n**Risk Management Workflow:**\n- Risk management planning and file establishment\n- Risk analysis and risk evaluation\n- Risk control implementation and verification\n- Production and post-production information analysis\n- Risk management file maintenance\n\n### Supplier Quality Management (ISO 13485 Clause 7.4)\nEstablish comprehensive supplier evaluation, selection, and monitoring processes.\n\n**Supplier Management Process:**\n- Supplier qualification and approval criteria\n- Performance monitoring and evaluation\n- Supplier audit programs\n- Supplier corrective action management\n- Supply chain risk assessment\n\n## QMS Performance Monitoring\n\n### Key Quality Indicators (KQIs)\nMonitor these critical quality metrics:\n- **QMS Process Performance**: Process cycle times, efficiency metrics\n- **Customer Satisfaction**: Complaint trends, satisfaction surveys\n- **Internal Audit Effectiveness**: Finding trends, closure rates\n- **CAPA Performance**: Closure timelines, effectiveness measures\n- **Training Effectiveness**: Competency assessments, compliance rates\n\n### Continuous Improvement\n**Improvement Methodology:**\n1. **Data Collection and Analysis**\n2. **Root Cause Analysis** using references\u002Froot-cause-analysis-tools.md\n3. **Improvement Planning** and resource allocation\n4. **Implementation and Monitoring**\n5. **Effectiveness Verification** and standardization\n\n## Regulatory Interface Management\n\n### ISO 13485 Certification Maintenance\n- Annual surveillance audit preparation\n- Certification body relationship management\n- Nonconformity resolution and follow-up\n- Certificate maintenance and renewal planning\n\n### QMS Integration with Regulatory Requirements\n- MDR Article 10 (Quality Management System) compliance\n- FDA 21 CFR 820 (Quality System Regulation) alignment\n- Other regulatory QMS requirements integration\n- Regulatory inspection readiness\n\n## Resources\n\n### scripts\u002F\n- `qms-performance-dashboard.py`: Automated QMS metrics tracking and reporting\n- `document-control-audit.py`: Document control compliance verification\n- `management-review-prep.py`: Management review input compilation automation\n- `audit-checklists\u002F`: Comprehensive internal audit checklist generators\n\n### references\u002F\n- `iso13485-procedures.md`: Standard operating procedures templates\n- `design-control-templates.md`: Design control documentation templates\n- `risk-management-integration.md`: ISO 14971 integration guidelines\n- `supplier-qualification-criteria.md`: Supplier assessment frameworks\n- `root-cause-analysis-tools.md`: Problem-solving methodologies\n\n### assets\u002F\n- `qms-templates\u002F`: Quality manual, procedure, and work instruction templates\n- `audit-forms\u002F`: Internal audit report and checklist templates\n- `training-materials\u002F`: ISO 13485 training presentations and materials\n- `process-flowcharts\u002F`: Visual process documentation templates\n",{"name":5,"description":7},"main","2b749c82b5d11fac39d9a6e021ce3f5b8a541bd1","cli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-manager-qms-iso13485",3931,"https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates","https:\u002F\u002Faitmpl.com","https:\u002F\u002Fgithub.com\u002Fdavila7","https:\u002F\u002Fdanielavila.me","Building AI dev tools with LLMs","2026-11-14 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quality-manager-qms-iso13485","安装技能，技能地址：https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-manager-qms-iso13485\u002FSKILL.md",true,[73,79,85],{"path":74,"resourceType":75,"resourceTypeDesc":76,"sizeBytes":77,"sourceHtmlUrl":78},"assets\u002Fexample_asset.txt","ASSET","资产文件",865,"https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-manager-qms-iso13485\u002Fassets\u002Fexample_asset.txt",{"path":80,"resourceType":81,"resourceTypeDesc":82,"sizeBytes":83,"sourceHtmlUrl":84},"references\u002Fapi_reference.md","REFERENCE","参考文档",979,"https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-manager-qms-iso13485\u002Freferences\u002Fapi_reference.md",{"path":86,"resourceType":87,"resourceTypeDesc":88,"sizeBytes":89,"sourceHtmlUrl":90},"scripts\u002Fexample.py","SCRIPT","脚本",615,"https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-manager-qms-iso13485\u002Fscripts\u002Fexample.py",[92,120,147,180,215,239],{"skillNo":93,"name":94,"nameZh":6,"description":95,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":96,"categories":97,"keywords":101,"publishedAt":44},"01M70NHBTQ8BV0A2SCAZXEPHCX","wealthville-pool-scoring","Score DeFi liquidity pools before providing liquidity. Returns a 0-100 pool score and an Enter\u002FHold\u002FExit\u002FReduce\u002FAvoid verdict with calibrated confidence for ~68,800 Solana pools and 575 EVM pools, plus a public miss-inclusive track record. Use when asked whether a pool is worth LPing into, which pools look best right now, or how accurate the scores have actually been.","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fweb-data\u002Fwealthville-pool-scoring\u002FSKILL.md",[98],{"categoryNo":99,"categoryName":100,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000023","Skill与智能体开发",[102,103,104,105,106,29,107,108,37,109,110,111,112,113,114,115,116,117,118,119],"scoring","pool","wealthville pool scoring","liquidity","which","exit","now","when","reduce","with","record","track","verdict","evm","solana","how","public","look",{"skillNo":121,"name":122,"nameZh":6,"description":123,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":124,"categories":125,"keywords":127,"publishedAt":44},"01M70MB6VR8ERJ4EM8D5KHBMEV","technical-debt-auditor","Scans a codebase and produces a quantified technical debt report with a prioritized remediation plan. Analyzes dead code, TODO\u002FFIXME\u002FHACK markers, dependency staleness, complexity hotspots, code duplication signals, test coverage gaps, unused exports, and outdated patterns. Use this skill when the user asks to audit their codebase for tech debt, wants a health check of their code quality, says things like \"where should I focus refactoring\", \"find code smells\", \"audit my codebase\", \"what technical debt do we have\", \"prioritize cleanup work\", or asks about code quality metrics. Also trigger when the user mentions \"code rot\", \"legacy cleanup\", \"refactoring priorities\", or wants to understand the overall health of a project before a major effort. Trigger even if the user doesn't say \"technical debt\" explicitly — any request to systematically assess code quality and identify improvement priorities belongs here.","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fdevelopment\u002Ftechnical-debt-auditor\u002FSKILL.md",[126],{"categoryNo":99,"categoryName":100,"taxonomyType":21,"taxonomyTypeDesc":22},[128,129,130,131,132,133,134,135,136,137,138,109,139,140,141,142,143,144,145,146],"technical debt","debt","technical","technical debt auditor","auditor","coverage","complexity","markers","project","cleanup","unused","code","todo","work","plan","focus","signals","audit","dependency",{"skillNo":148,"name":149,"nameZh":6,"description":150,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":151,"categories":152,"keywords":162,"publishedAt":44},"01M70KPYH9QNHCNME5GJQGE22K","readonly-sql-guard","Make an agent's database access provably read-only. Use when an agent runs caller-supplied SQL against a production\u002FERP\u002Fanalytics database (a \"query\" MCP tool, text-to-SQL, an admin console), or when reviewing DB-access code for write\u002FDDL\u002Fside-effect\u002Ftransaction-escape risks. Checks what a statement CALLS, not just its shape.","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fdatabase\u002Freadonly-sql-guard\u002FSKILL.md",[153,156,157],{"categoryNo":154,"categoryName":155,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000010","后端与接口",{"categoryNo":99,"categoryName":100,"taxonomyType":21,"taxonomyTypeDesc":22},{"categoryNo":158,"categoryName":159,"taxonomyType":160,"taxonomyTypeDesc":161},"01JBSEEDCAT000000000000033","数据分析师","PROFESSION","适用职业",[163,164,165,166,167,168,169,29,170,171,172,173,174,175,176,37,177,178,109,179],"readonly","guard","sql guard","sql","readonly sql guard","erp","effect","read-only","db","just","tool","calls","only","MCP","access","database","query",{"skillNo":181,"name":182,"nameZh":6,"description":183,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":184,"licenseFileUrl":185,"sourceHtmlUrl":186,"categories":187,"keywords":191,"publishedAt":44},"01M6AFY6F7CC2BBZP1QD6VTNVC","web-artifacts-builder","Suite of tools for creating elaborate, multi-component claude.ai HTML artifacts using modern frontend web technologies (React, Tailwind CSS, shadcn\u002Fui). 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