[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"skill:01M6AF2NSWGEFQC9ZEV49CNZ2V":3,"skill-same:01M6AF2NSWGEFQC9ZEV49CNZ2V":120},{"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":28,"publishedAt":50,"linkOnly":51,"markdownContent":52,"markdownBody":53,"frontMatter":54,"refName":55,"commitSha":56,"skillDirectory":57,"forksCount":58,"repositoryHtmlUrl":59,"repositoryHomepageUrl":60,"ownerHtmlUrl":61,"ownerBlogUrl":62,"ownerDescription":63,"updatedAt":64,"install":65,"resources":78},"01M6AF2NSWGEFQC9ZEV49CNZ2V","quality-documentation-manager",null,"Senior Quality Documentation Manager for comprehensive documentation control and regulatory document review. Provides document management system design, change control, configuration management, and regulatory documentation oversight. Use for document control system implementation, regulatory document review, change management, and documentation compliance verification.","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-documentation-manager\u002FSKILL.md",[18,23],{"categoryNo":19,"categoryName":20,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000015","视觉设计","SCENARIO","使用场景",{"categoryNo":24,"categoryName":25,"taxonomyType":26,"taxonomyTypeDesc":27},"01JBSEEDCAT000000000000037","律师与法务","PROFESSION","适用职业",[29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49],"documentation","manager","quality documentation manager","quality","oversight","document management","senior","for","change control","document review","configuration management","document","system design","use","design","change management","system","compliance","verification","change","review","2026-11-10 10:12:30",false,"---\nname: quality-documentation-manager\ndescription: Senior Quality Documentation Manager for comprehensive documentation control and regulatory document review. Provides document management system design, change control, configuration management, and regulatory documentation oversight. Use for document control system implementation, regulatory document review, change management, and documentation compliance verification.\n---\n\n# Senior Quality Documentation Manager\n\nExpert-level quality documentation management with comprehensive document control system design, regulatory documentation oversight, change management, and configuration control for medical device organizations.\n\n## Core Documentation Management Competencies\n\n### 1. Document Control System Design (ISO 13485 Clause 4.2.3)\nDesign and implement comprehensive document control systems ensuring systematic document management and regulatory compliance.\n\n**Document Control System Framework:**\n```\nDOCUMENT CONTROL SYSTEM ARCHITECTURE\n├── Document Classification and Structure\n│   ├── Document type taxonomy and hierarchy\n│   ├── Document numbering and identification\n│   ├── Version control and revision management\n│   └── Document status and lifecycle tracking\n├── Document Creation and Approval\n│   ├── Document templates and standardization\n│   ├── Review and approval workflows\n│   ├── Author and reviewer role assignment\n│   └── Quality assurance and validation\n├── Document Distribution and Access\n│   ├── Controlled distribution management\n│   ├── Access permission and security\n│   ├── Electronic document system integration\n│   └── External document coordination\n├── Document Maintenance and Updates\n│   ├── Periodic review scheduling\n│   ├── Change control procedures\n│   ├── Impact assessment and validation\n│   └── Obsolete document management\n└── Document Retention and Disposal\n    ├── Retention period determination\n    ├── Archive management system\n    ├── Legal hold and litigation support\n    └── Secure disposal procedures\n```\n\n### 2. Regulatory Documentation Oversight\nProvide comprehensive oversight of regulatory documentation ensuring compliance with multiple jurisdictional requirements.\n\n**Regulatory Documentation Framework:**\n1. **Multi-jurisdictional Documentation Management**\n   - **EU MDR Technical Documentation**: Annex II and III compliance verification\n   - **FDA Submission Documentation**: 510(k), PMA, and De Novo documentation oversight\n   - **ISO Standard Documentation**: ISO 13485, ISO 14971, and related standard compliance\n   - **International Market Documentation**: Health Canada, TGA, and other market requirements\n\n2. **Documentation Quality Assurance**\n   - **Content Review and Validation**: Technical accuracy and regulatory compliance\n   - **Format and Structure Verification**: Regulatory template and guideline adherence\n   - **Cross-reference and Traceability**: Document linkage and relationship management\n   - **Decision Point**: Approve documentation for regulatory submission or internal use\n\n3. **Regulatory Submission Coordination**\n   - **Submission Package Assembly**: Document compilation and organization\n   - **Regulatory Authority Communication**: Documentation-related queries and responses\n   - **Post-submission Updates**: Amendment and variation documentation\n   - **Market Access Documentation**: Product registration and certification support\n\n### 3. Change Control and Configuration Management\nImplement robust change control processes ensuring systematic document change management and configuration control.\n\n**Change Control Process Framework:**\n```\nDOCUMENT CHANGE CONTROL WORKFLOW\n├── Change Request Initiation\n│   ├── Change identification and justification\n│   ├── Impact assessment and analysis\n│   ├── Stakeholder notification and consultation\n│   └── Change request documentation\n├── Change Review and Approval\n│   ├── Technical review and validation\n│   ├── Regulatory impact assessment\n│   ├── Risk assessment and mitigation\n│   ├── Resource requirement evaluation\n│   └── Change approval authorization\n├── Change Implementation\n│   ├── Document update and revision\n│   ├── Training and communication\n│   ├── System update and deployment\n│   └── Verification and validation\n├── Change Verification and Closure\n│   ├── Implementation verification\n│   ├── Effectiveness assessment\n│   ├── Stakeholder confirmation\n│   └── Change record completion\n└── Post-Change Monitoring\n    ├── Performance monitoring\n    ├── Issue identification and resolution\n    ├── Lessons learned capture\n    └── Process improvement integration\n```\n\n### 4. Document Management System (DMS) Implementation\nDesign and implement comprehensive electronic document management systems ensuring efficient document operations and compliance.\n\n**DMS Implementation Strategy:**\n1. **System Requirements and Selection**\n   - Functional requirement definition and validation\n   - Regulatory compliance requirement integration\n   - System evaluation and vendor selection\n   - **Decision Point**: Select DMS technology and implementation approach\n\n2. **System Design and Configuration**\n   - **For Document Storage**: Follow references\u002Fdms-storage-design.md\n   - **For Workflow Management**: Follow references\u002Fworkflow-automation.md\n   - **For Integration**: Follow references\u002Fsystem-integration-guide.md\n   - User interface design and experience optimization\n\n3. **System Validation and Deployment**\n   - System testing and validation protocols\n   - User training and competency verification\n   - Phased rollout and change management\n   - Performance monitoring and optimization\n\n## Advanced Documentation Applications\n\n### Technical Documentation Management\nManage complex technical documentation ensuring accuracy, consistency, and regulatory compliance.\n\n**Technical Documentation Categories:**\n- **Design and Development Documentation**: Design inputs, outputs, reviews, verification, validation\n- **Risk Management Documentation**: ISO 14971 risk management file and reports\n- **Clinical Documentation**: Clinical evaluation reports, clinical investigation protocols\n- **Manufacturing Documentation**: Process specifications, work instructions, validation reports\n- **Post-Market Documentation**: Surveillance reports, vigilance documentation, CAPA records\n\n### Electronic Signature and 21 CFR Part 11 Compliance\nImplement electronic signature systems ensuring FDA 21 CFR Part 11 compliance and regulatory acceptance.\n\n**Electronic Signature Framework:**\n1. **21 CFR Part 11 Compliance Implementation**\n   - Electronic signature system validation and qualification\n   - User authentication and authorization management\n   - Audit trail and system security implementation\n   - **System Controls**: Access controls, operational controls, authority checks\n\n2. **Electronic Record Management**\n   - Electronic record integrity and authenticity\n   - Record retention and archive management\n   - System migration and legacy data management\n   - Regulatory inspection readiness and support\n\n### Multi-language Documentation Management\nManage multi-language documentation ensuring consistency, accuracy, and regulatory compliance across global markets.\n\n**Multi-language Documentation Strategy:**\n- **Translation Management**: Professional translation coordination and quality assurance\n- **Linguistic Validation**: Medical and technical terminology accuracy verification\n- **Cultural Adaptation**: Local market requirement integration and customization\n- **Version Synchronization**: Multi-language document version control and alignment\n\n## Document Control Performance and Quality\n\n### Documentation Quality Metrics\nMonitor comprehensive documentation quality metrics ensuring continuous improvement and regulatory compliance.\n\n**Documentation Quality KPIs:**\n- **Document Accuracy**: Error rates, correction frequency, review effectiveness\n- **Compliance Rate**: Regulatory requirement adherence and audit findings\n- **Process Efficiency**: Document cycle times, approval durations, update frequencies\n- **User Satisfaction**: Stakeholder feedback, usability assessment, training effectiveness\n- **System Performance**: DMS uptime, access speed, search effectiveness\n\n### Document Control Audit and Assessment\nConduct systematic document control audits ensuring compliance and continuous improvement.\n\n**Document Control Audit Framework:**\n1. **Document Control System Assessment**\n   - Document control procedure compliance verification\n   - System functionality and performance evaluation\n   - User competency and training assessment\n   - **Regulatory Compliance Verification**: Multi-jurisdictional requirement adherence\n\n2. **Documentation Quality Review**\n   - Document accuracy and completeness assessment\n   - Regulatory compliance and guideline adherence\n   - Cross-reference and traceability verification\n   - Version control and change management effectiveness\n\n### Continuous Improvement and Optimization\nImplement continuous improvement processes ensuring document control system optimization and stakeholder satisfaction.\n\n**Improvement Framework:**\n- **Process Optimization**: Workflow streamlining and automation opportunities\n- **Technology Enhancement**: System upgrade and functionality improvement\n- **User Experience Improvement**: Interface optimization and training effectiveness\n- **Regulatory Alignment**: Evolving regulatory requirement integration and compliance\n\n## Cross-functional Documentation Coordination\n\n### Quality System Integration\nEnsure seamless integration of documentation management with quality management system processes.\n\n**QMS Integration Points:**\n- **Management Review**: Documentation performance reporting and metrics\n- **Internal Audit**: Document control compliance verification and improvement\n- **CAPA Integration**: Documentation-related corrective and preventive actions\n- **Training Management**: Document-based training and competency verification\n\n### Regulatory Affairs Coordination\nCoordinate closely with regulatory affairs team ensuring regulatory documentation accuracy and compliance.\n\n**Regulatory Coordination Framework:**\n- **Submission Support**: Regulatory documentation preparation and quality assurance\n- **Regulatory Intelligence**: Guidance document monitoring and implementation\n- **Authority Communication**: Documentation-related query response and clarification\n- **Compliance Monitoring**: Multi-jurisdictional documentation requirement tracking\n\n### Cross-functional Training and Support\nProvide comprehensive training and support ensuring organizational document management competency.\n\n**Training and Support Program:**\n- **Document Author Training**: Document creation, review, and approval procedures\n- **System User Training**: DMS functionality and best practice utilization\n- **Regulatory Documentation Training**: Specific regulatory requirement and guideline training\n- **Ongoing Support**: Help desk, troubleshooting, and continuous learning support\n\n## Regulatory Documentation Standards\n\n### International Documentation Standards\nEnsure compliance with international documentation standards and regulatory expectations.\n\n**Standards Compliance Framework:**\n- **ISO 13485 Documentation**: Quality management system documentation requirements\n- **IEC 62304 Documentation**: Medical device software lifecycle documentation\n- **ISO 14971 Documentation**: Risk management documentation and reporting\n- **ICH Guidelines**: Clinical documentation standards and harmonization\n\n### Documentation Best Practices\nImplement industry best practices ensuring documentation excellence and regulatory acceptance.\n\n**Best Practice Implementation:**\n- **Plain Language**: Clear, concise, and understandable documentation\n- **Visual Communication**: Diagrams, flowcharts, and graphical representations\n- **Modular Design**: Reusable documentation components and templates\n- **Accessibility**: Universal design and multi-format accessibility\n\n## Resources\n\n### scripts\u002F\n- `document-control-dashboard.py`: Comprehensive document management performance monitoring\n- `change-control-automation.py`: Document change workflow automation and tracking\n- `regulatory-doc-validator.py`: Regulatory documentation compliance verification\n- `dms-performance-monitor.py`: Document management system performance optimization\n\n### references\u002F\n- `document-control-procedures.md`: Comprehensive document control implementation guide\n- `regulatory-documentation-standards.md`: Multi-jurisdictional documentation requirements\n- `dms-storage-design.md`: Document management system architecture and design\n- `workflow-automation.md`: Document workflow optimization and automation\n- `21cfr11-compliance-guide.md`: Electronic signature and record compliance framework\n\n### assets\u002F\n- `document-templates\u002F`: Standardized document templates and formats\n- `change-control-forms\u002F`: Change request and approval documentation templates\n- `training-materials\u002F`: Document management training and competency programs\n- `audit-checklists\u002F`: Document control compliance verification checklists\n","# Senior Quality Documentation Manager\n\nExpert-level quality documentation management with comprehensive document control system design, regulatory documentation oversight, change management, and configuration control for medical device organizations.\n\n## Core Documentation Management Competencies\n\n### 1. Document Control System Design (ISO 13485 Clause 4.2.3)\nDesign and implement comprehensive document control systems ensuring systematic document management and regulatory compliance.\n\n**Document Control System Framework:**\n```\nDOCUMENT CONTROL SYSTEM ARCHITECTURE\n├── Document Classification and Structure\n│   ├── Document type taxonomy and hierarchy\n│   ├── Document numbering and identification\n│   ├── Version control and revision management\n│   └── Document status and lifecycle tracking\n├── Document Creation and Approval\n│   ├── Document templates and standardization\n│   ├── Review and approval workflows\n│   ├── Author and reviewer role assignment\n│   └── Quality assurance and validation\n├── Document Distribution and Access\n│   ├── Controlled distribution management\n│   ├── Access permission and security\n│   ├── Electronic document system integration\n│   └── External document coordination\n├── Document Maintenance and Updates\n│   ├── Periodic review scheduling\n│   ├── Change control procedures\n│   ├── Impact assessment and validation\n│   └── Obsolete document management\n└── Document Retention and Disposal\n    ├── Retention period determination\n    ├── Archive management system\n    ├── Legal hold and litigation support\n    └── Secure disposal procedures\n```\n\n### 2. Regulatory Documentation Oversight\nProvide comprehensive oversight of regulatory documentation ensuring compliance with multiple jurisdictional requirements.\n\n**Regulatory Documentation Framework:**\n1. **Multi-jurisdictional Documentation Management**\n   - **EU MDR Technical Documentation**: Annex II and III compliance verification\n   - **FDA Submission Documentation**: 510(k), PMA, and De Novo documentation oversight\n   - **ISO Standard Documentation**: ISO 13485, ISO 14971, and related standard compliance\n   - **International Market Documentation**: Health Canada, TGA, and other market requirements\n\n2. **Documentation Quality Assurance**\n   - **Content Review and Validation**: Technical accuracy and regulatory compliance\n   - **Format and Structure Verification**: Regulatory template and guideline adherence\n   - **Cross-reference and Traceability**: Document linkage and relationship management\n   - **Decision Point**: Approve documentation for regulatory submission or internal use\n\n3. **Regulatory Submission Coordination**\n   - **Submission Package Assembly**: Document compilation and organization\n   - **Regulatory Authority Communication**: Documentation-related queries and responses\n   - **Post-submission Updates**: Amendment and variation documentation\n   - **Market Access Documentation**: Product registration and certification support\n\n### 3. Change Control and Configuration Management\nImplement robust change control processes ensuring systematic document change management and configuration control.\n\n**Change Control Process Framework:**\n```\nDOCUMENT CHANGE CONTROL WORKFLOW\n├── Change Request Initiation\n│   ├── Change identification and justification\n│   ├── Impact assessment and analysis\n│   ├── Stakeholder notification and consultation\n│   └── Change request documentation\n├── Change Review and Approval\n│   ├── Technical review and validation\n│   ├── Regulatory impact assessment\n│   ├── Risk assessment and mitigation\n│   ├── Resource requirement evaluation\n│   └── Change approval authorization\n├── Change Implementation\n│   ├── Document update and revision\n│   ├── Training and communication\n│   ├── System update and deployment\n│   └── Verification and validation\n├── Change Verification and Closure\n│   ├── Implementation verification\n│   ├── Effectiveness assessment\n│   ├── Stakeholder confirmation\n│   └── Change record completion\n└── Post-Change Monitoring\n    ├── Performance monitoring\n    ├── Issue identification and resolution\n    ├── Lessons learned capture\n    └── Process improvement integration\n```\n\n### 4. Document Management System (DMS) Implementation\nDesign and implement comprehensive electronic document management systems ensuring efficient document operations and compliance.\n\n**DMS Implementation Strategy:**\n1. **System Requirements and Selection**\n   - Functional requirement definition and validation\n   - Regulatory compliance requirement integration\n   - System evaluation and vendor selection\n   - **Decision Point**: Select DMS technology and implementation approach\n\n2. **System Design and Configuration**\n   - **For Document Storage**: Follow references\u002Fdms-storage-design.md\n   - **For Workflow Management**: Follow references\u002Fworkflow-automation.md\n   - **For Integration**: Follow references\u002Fsystem-integration-guide.md\n   - User interface design and experience optimization\n\n3. **System Validation and Deployment**\n   - System testing and validation protocols\n   - User training and competency verification\n   - Phased rollout and change management\n   - Performance monitoring and optimization\n\n## Advanced Documentation Applications\n\n### Technical Documentation Management\nManage complex technical documentation ensuring accuracy, consistency, and regulatory compliance.\n\n**Technical Documentation Categories:**\n- **Design and Development Documentation**: Design inputs, outputs, reviews, verification, validation\n- **Risk Management Documentation**: ISO 14971 risk management file and reports\n- **Clinical Documentation**: Clinical evaluation reports, clinical investigation protocols\n- **Manufacturing Documentation**: Process specifications, work instructions, validation reports\n- **Post-Market Documentation**: Surveillance reports, vigilance documentation, CAPA records\n\n### Electronic Signature and 21 CFR Part 11 Compliance\nImplement electronic signature systems ensuring FDA 21 CFR Part 11 compliance and regulatory acceptance.\n\n**Electronic Signature Framework:**\n1. **21 CFR Part 11 Compliance Implementation**\n   - Electronic signature system validation and qualification\n   - User authentication and authorization management\n   - Audit trail and system security implementation\n   - **System Controls**: Access controls, operational controls, authority checks\n\n2. **Electronic Record Management**\n   - Electronic record integrity and authenticity\n   - Record retention and archive management\n   - System migration and legacy data management\n   - Regulatory inspection readiness and support\n\n### Multi-language Documentation Management\nManage multi-language documentation ensuring consistency, accuracy, and regulatory compliance across global markets.\n\n**Multi-language Documentation Strategy:**\n- **Translation Management**: Professional translation coordination and quality assurance\n- **Linguistic Validation**: Medical and technical terminology accuracy verification\n- **Cultural Adaptation**: Local market requirement integration and customization\n- **Version Synchronization**: Multi-language document version control and alignment\n\n## Document Control Performance and Quality\n\n### Documentation Quality Metrics\nMonitor comprehensive documentation quality metrics ensuring continuous improvement and regulatory compliance.\n\n**Documentation Quality KPIs:**\n- **Document Accuracy**: Error rates, correction frequency, review effectiveness\n- **Compliance Rate**: Regulatory requirement adherence and audit findings\n- **Process Efficiency**: Document cycle times, approval durations, update frequencies\n- **User Satisfaction**: Stakeholder feedback, usability assessment, training effectiveness\n- **System Performance**: DMS uptime, access speed, search effectiveness\n\n### Document Control Audit and Assessment\nConduct systematic document control audits ensuring compliance and continuous improvement.\n\n**Document Control Audit Framework:**\n1. **Document Control System Assessment**\n   - Document control procedure compliance verification\n   - System functionality and performance evaluation\n   - User competency and training assessment\n   - **Regulatory Compliance Verification**: Multi-jurisdictional requirement adherence\n\n2. **Documentation Quality Review**\n   - Document accuracy and completeness assessment\n   - Regulatory compliance and guideline adherence\n   - Cross-reference and traceability verification\n   - Version control and change management effectiveness\n\n### Continuous Improvement and Optimization\nImplement continuous improvement processes ensuring document control system optimization and stakeholder satisfaction.\n\n**Improvement Framework:**\n- **Process Optimization**: Workflow streamlining and automation opportunities\n- **Technology Enhancement**: System upgrade and functionality improvement\n- **User Experience Improvement**: Interface optimization and training effectiveness\n- **Regulatory Alignment**: Evolving regulatory requirement integration and compliance\n\n## Cross-functional Documentation Coordination\n\n### Quality System Integration\nEnsure seamless integration of documentation management with quality management system processes.\n\n**QMS Integration Points:**\n- **Management Review**: Documentation performance reporting and metrics\n- **Internal Audit**: Document control compliance verification and improvement\n- **CAPA Integration**: Documentation-related corrective and preventive actions\n- **Training Management**: Document-based training and competency verification\n\n### Regulatory Affairs Coordination\nCoordinate closely with regulatory affairs team ensuring regulatory documentation accuracy and compliance.\n\n**Regulatory Coordination Framework:**\n- **Submission Support**: Regulatory documentation preparation and quality assurance\n- **Regulatory Intelligence**: Guidance document monitoring and implementation\n- **Authority Communication**: Documentation-related query response and clarification\n- **Compliance Monitoring**: Multi-jurisdictional documentation requirement tracking\n\n### Cross-functional Training and Support\nProvide comprehensive training and support ensuring organizational document management competency.\n\n**Training and Support Program:**\n- **Document Author Training**: Document creation, review, and approval procedures\n- **System User Training**: DMS functionality and best practice utilization\n- **Regulatory Documentation Training**: Specific regulatory requirement and guideline training\n- **Ongoing Support**: Help desk, troubleshooting, and continuous learning support\n\n## Regulatory Documentation Standards\n\n### International Documentation Standards\nEnsure compliance with international documentation standards and regulatory expectations.\n\n**Standards Compliance Framework:**\n- **ISO 13485 Documentation**: Quality management system documentation requirements\n- **IEC 62304 Documentation**: Medical device software lifecycle documentation\n- **ISO 14971 Documentation**: Risk management documentation and reporting\n- **ICH Guidelines**: Clinical documentation standards and harmonization\n\n### Documentation Best Practices\nImplement industry best practices ensuring documentation excellence and regulatory acceptance.\n\n**Best Practice Implementation:**\n- **Plain Language**: Clear, concise, and understandable documentation\n- **Visual Communication**: Diagrams, flowcharts, and graphical representations\n- **Modular Design**: Reusable documentation components and templates\n- **Accessibility**: Universal design and multi-format accessibility\n\n## Resources\n\n### scripts\u002F\n- `document-control-dashboard.py`: Comprehensive document management performance monitoring\n- `change-control-automation.py`: Document change workflow automation and tracking\n- `regulatory-doc-validator.py`: Regulatory documentation compliance verification\n- `dms-performance-monitor.py`: Document management system performance optimization\n\n### references\u002F\n- `document-control-procedures.md`: Comprehensive document control implementation guide\n- `regulatory-documentation-standards.md`: Multi-jurisdictional documentation requirements\n- `dms-storage-design.md`: Document management system architecture and design\n- `workflow-automation.md`: Document workflow optimization and automation\n- `21cfr11-compliance-guide.md`: Electronic signature and record compliance framework\n\n### assets\u002F\n- `document-templates\u002F`: Standardized document templates and formats\n- `change-control-forms\u002F`: Change request and approval documentation templates\n- `training-materials\u002F`: Document management training and competency programs\n- `audit-checklists\u002F`: Document control compliance verification checklists\n",{"name":5,"description":7},"main","2b749c82b5d11fac39d9a6e021ce3f5b8a541bd1","cli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-documentation-manager",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 06:14:46",{"source":8,"skillName":5,"commands":66,"prompt":76,"zipAvailable":77},[67,70,73],{"tool":68,"command":69},"npx","npx skills add davila7\u002Fclaude-code-templates --skill quality-documentation-manager",{"tool":71,"command":72},"bunx","bunx skills add davila7\u002Fclaude-code-templates --skill quality-documentation-manager",{"tool":74,"command":75},"pnpm","pnpm dlx skills add davila7\u002Fclaude-code-templates --skill quality-documentation-manager","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-documentation-manager\u002FSKILL.md",true,[79,85,91,95,98,102,108,112,116],{"path":80,"resourceType":81,"resourceTypeDesc":82,"sizeBytes":83,"sourceHtmlUrl":84},"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-documentation-manager\u002Fassets\u002Fexample_asset.txt",{"path":86,"resourceType":87,"resourceTypeDesc":88,"sizeBytes":89,"sourceHtmlUrl":90},"references\u002Fapi_reference.md","REFERENCE","参考文档",980,"https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-documentation-manager\u002Freferences\u002Fapi_reference.md",{"path":92,"resourceType":87,"resourceTypeDesc":88,"sizeBytes":93,"sourceHtmlUrl":94},"references\u002Fcomputer_vision_architectures.md",1447,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fengineering-team\u002Fsenior-computer-vision\u002Freferences\u002Fcomputer_vision_architectures.md",{"path":96,"resourceType":87,"resourceTypeDesc":88,"sizeBytes":93,"sourceHtmlUrl":97},"references\u002Fobject_detection_optimization.md","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fengineering-team\u002Fsenior-computer-vision\u002Freferences\u002Fobject_detection_optimization.md",{"path":99,"resourceType":87,"resourceTypeDesc":88,"sizeBytes":100,"sourceHtmlUrl":101},"references\u002Fproduction_vision_systems.md",1439,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fengineering-team\u002Fsenior-computer-vision\u002Freferences\u002Fproduction_vision_systems.md",{"path":103,"resourceType":104,"resourceTypeDesc":105,"sizeBytes":106,"sourceHtmlUrl":107},"scripts\u002Fdataset_pipeline_builder.py","SCRIPT","脚本",2817,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fengineering-team\u002Fsenior-computer-vision\u002Fscripts\u002Fdataset_pipeline_builder.py",{"path":109,"resourceType":104,"resourceTypeDesc":105,"sizeBytes":110,"sourceHtmlUrl":111},"scripts\u002Fexample.py",617,"https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fenterprise-communication\u002Fquality-documentation-manager\u002Fscripts\u002Fexample.py",{"path":113,"resourceType":104,"resourceTypeDesc":105,"sizeBytes":114,"sourceHtmlUrl":115},"scripts\u002Finference_optimizer.py",2794,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fengineering-team\u002Fsenior-computer-vision\u002Fscripts\u002Finference_optimizer.py",{"path":117,"resourceType":104,"resourceTypeDesc":105,"sizeBytes":118,"sourceHtmlUrl":119},"scripts\u002Fvision_model_trainer.py",2797,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fengineering-team\u002Fsenior-computer-vision\u002Fscripts\u002Fvision_model_trainer.py",[121,149,176,207,242,266],{"skillNo":122,"name":123,"nameZh":6,"description":124,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":125,"categories":126,"keywords":130,"publishedAt":50},"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",[127],{"categoryNo":128,"categoryName":129,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000023","Skill与智能体开发",[131,132,133,134,135,36,136,137,42,138,139,140,141,142,143,144,145,146,147,148],"scoring","pool","wealthville pool scoring","liquidity","which","exit","now","when","reduce","with","record","track","verdict","evm","solana","how","public","look",{"skillNo":150,"name":151,"nameZh":6,"description":152,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":153,"categories":154,"keywords":156,"publishedAt":50},"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",[155],{"categoryNo":128,"categoryName":129,"taxonomyType":21,"taxonomyTypeDesc":22},[157,158,159,160,161,162,163,164,165,166,167,138,168,169,170,171,172,173,174,175],"technical debt","debt","technical","technical debt auditor","auditor","coverage","complexity","markers","project","cleanup","unused","code","todo","work","plan","focus","signals","audit","dependency",{"skillNo":177,"name":178,"nameZh":6,"description":179,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":180,"categories":181,"keywords":189,"publishedAt":50},"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",[182,185,186],{"categoryNo":183,"categoryName":184,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000010","后端与接口",{"categoryNo":128,"categoryName":129,"taxonomyType":21,"taxonomyTypeDesc":22},{"categoryNo":187,"categoryName":188,"taxonomyType":26,"taxonomyTypeDesc":27},"01JBSEEDCAT000000000000033","数据分析师",[190,191,192,193,194,195,196,36,197,198,199,200,201,202,203,42,204,205,138,206],"readonly","guard","sql guard","sql","readonly sql guard","erp","effect","read-only","db","just","tool","calls","only","MCP","access","database","query",{"skillNo":208,"name":209,"nameZh":6,"description":210,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":211,"licenseFileUrl":212,"sourceHtmlUrl":213,"categories":214,"keywords":218,"publishedAt":50},"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). Use for complex artifacts requiring state management, routing, or shadcn\u002Fui components - not for simple single-file HTML\u002FJSX artifacts.","Apache-2.0","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Futilities\u002Fweb-artifacts-builder\u002FLICENSE.txt","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Futilities\u002Fweb-artifacts-builder\u002FSKILL.md",[215],{"categoryNo":216,"categoryName":217,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000009","前端开发",[219,220,221,222,223,224,225,226,227,228,229,230,231,232,233,234,235,236,237,238,239,240,36,241],"artifacts builder","web","web artifacts builder","artifacts","builder","state","routing","state management","component","css","frontend","ui","Tools","file","components","shadcn","react","Tailwind","suite","jsx","html","single-file","ui components",{"skillNo":243,"name":244,"nameZh":6,"description":245,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":211,"licenseFileUrl":246,"sourceHtmlUrl":247,"categories":248,"keywords":253,"publishedAt":50},"01M6AFWF33SFV9Z3SF4PEEE4BF","webapp-testing","Toolkit for interacting with and testing local web applications using Playwright. Supports verifying frontend functionality, debugging UI behavior, capturing browser screenshots, and viewing browser logs.","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fsecurity\u002Fwebapp-testing\u002FLICENSE.txt","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fsecurity\u002Fwebapp-testing\u002FSKILL.md",[249,252],{"categoryNo":250,"categoryName":251,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000008","测试与质量",{"categoryNo":216,"categoryName":217,"taxonomyType":21,"taxonomyTypeDesc":22},[254,255,256,257,258,220,259,229,230,260,261,262,263,36,264,140,265],"webapp testing","testing","webapp","browser","playwright","applications","debugging","toolkit","logs","screenshots","local","behavior",{"skillNo":267,"name":268,"nameZh":6,"description":269,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":211,"licenseFileUrl":270,"sourceHtmlUrl":271,"categories":272,"keywords":280,"publishedAt":50},"01M6AF67Q67JJJ5V51JR2P52KA","discernment-nudge","After you give a substantive answer or draft that the user may act on — advice or recommendations, drafted artifacts such as goals, plans, pitches, proposals, or emails, estimates or projections, analysis or interpretation of data, factual claims they may rely on, or a multi-step argument — invoke this skill BEFORE finalizing your reply and then, if it applies, append 2-3 short follow-up questions, each tied to something specific in what you just produced, that help the user check key facts, probe the reasoning or assumptions, and notice missing context. Do this at most once per conversation. Skip it when the user asked a trivial how-to or simple lookup, wants a purely educational explanation, asked you only to format, convert, or assemble a file from content they provided, is writing code they will run, is doing creative writing or casual chat, or already asked you to double-check, cite, or review — the skill file explains these boundaries and the exact output format.","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fproductivity\u002Fdiscernment-nudge\u002FLICENSE.txt","https:\u002F\u002Fgithub.com\u002Fdavila7\u002Fclaude-code-templates\u002Fblob\u002Fmain\u002Fcli-tool\u002Fcomponents\u002Fskills\u002Fproductivity\u002Fdiscernment-nudge\u002FSKILL.md",[273,276,277],{"categoryNo":274,"categoryName":275,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000018","写作与文案",{"categoryNo":128,"categoryName":129,"taxonomyType":21,"taxonomyTypeDesc":22},{"categoryNo":278,"categoryName":279,"taxonomyType":26,"taxonomyTypeDesc":27},"01JBSEEDCAT000000000000036","内容创作者",[281,282,283,284,285,286,287,288,222,289,232,168,290,49,291,292,293,202,294,138,295,296,297,298,299,146,300],"discernment nudge","nudge","interpretation","help","run","reasoning","data","writing","lookup","content","conversation","short","up","invoke","you","analysis","claims","argument","assemble","recommendations"]