[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"skill:01M70HG70Q5KSW723NMSVZA2VT":3,"skill-same:01M70HG70Q5KSW723NMSVZA2VT":96},{"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":49,"linkOnly":50,"markdownContent":51,"markdownBody":52,"frontMatter":53,"refName":54,"commitSha":55,"skillDirectory":56,"forksCount":57,"repositoryHtmlUrl":58,"repositoryHomepageUrl":59,"ownerHtmlUrl":60,"ownerBlogUrl":61,"ownerDescription":62,"updatedAt":63,"install":64,"resources":77},"01M70HG70Q5KSW723NMSVZA2VT","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.","shengdabai\u002FTony-Claude-Code-Skills","shengdabai","https:\u002F\u002Favatars.githubusercontent.com\u002Fu\u002F116417419?v=4","01M70F6D2WY5PQV5A92BKYJQEW","Tony Sheng","01M70F6D3GAAAYZ5H4CC1G8VXM",3,"MIT","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002F_collections\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fra-qm-team\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],"documentation","manager","quality","quality documentation manager","document","use","system","for","configuration management","senior","change control","change","verification","review","document review","design","change management","document management","system design","oversight","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","7850740bd837adb32f0a109ab2af82482196c6f2","skills\u002F_collections\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fra-qm-team\u002Fquality-documentation-manager",1,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills","https:\u002F\u002Fzturnsgo.com","https:\u002F\u002Fgithub.com\u002Fshengdabai","https:\u002F\u002Fzturnsgo.com\u002F","AI × education creator — producer, not consumer. Taught 6,000+ learners; shipping learning tools & daily essays with Claude Code, practicing @xiaolai's way 🥋","2026-11-01 21:28:23",{"source":8,"skillName":5,"commands":65,"prompt":75,"zipAvailable":76},[66,69,72],{"tool":67,"command":68},"npx","npx skills add shengdabai\u002FTony-Claude-Code-Skills --skill quality-documentation-manager",{"tool":70,"command":71},"bunx","bunx skills add shengdabai\u002FTony-Claude-Code-Skills --skill quality-documentation-manager",{"tool":73,"command":74},"pnpm","pnpm dlx skills add shengdabai\u002FTony-Claude-Code-Skills --skill quality-documentation-manager","安装技能，技能地址：https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002F_collections\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fra-qm-team\u002Fquality-documentation-manager\u002FSKILL.md",true,[78,84,90],{"path":79,"resourceType":80,"resourceTypeDesc":81,"sizeBytes":82,"sourceHtmlUrl":83},"assets\u002Fexample_asset.txt","ASSET","资产文件",865,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002F_collections\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fra-qm-team\u002Fquality-documentation-manager\u002Fassets\u002Fexample_asset.txt",{"path":85,"resourceType":86,"resourceTypeDesc":87,"sizeBytes":88,"sourceHtmlUrl":89},"references\u002Fapi_reference.md","REFERENCE","参考文档",980,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002F_collections\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fra-qm-team\u002Fquality-documentation-manager\u002Freferences\u002Fapi_reference.md",{"path":91,"resourceType":92,"resourceTypeDesc":93,"sizeBytes":94,"sourceHtmlUrl":95},"scripts\u002Fexample.py","SCRIPT","脚本",617,"https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002F_collections\u002Frsmdt-the-startup\u002Falirezarezvani-claude-skills\u002Fra-qm-team\u002Fquality-documentation-manager\u002Fscripts\u002Fexample.py",[97,114,145,171,193,213],{"skillNo":98,"name":99,"nameZh":6,"description":100,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":101,"categories":102,"keywords":106,"publishedAt":49},"01M70P17DAD4C1C47NPH6A96EM","xiaolai-methodology","以李笑来(Li Xiaolai)的思考方式、方法论与表达风格,为用户做全方位 1-on-1 教练指导,覆盖创业、赚钱、投资、学习、自学、读书写作、用 AI、以及人生心态与自我管理。当用户提到 \"李笑来\"、\"笑来\"、\"笑来老师\"、\"扮演李笑来\"、\"找笑来聊聊\"、\"笑来怎么看\"、\"xiaolai\"、\"把时间当作朋友\"、\"通往财富自由之路\"、\"定投改变命运\"、\"韭菜的自我修养\"、\"自学是门手艺\"、\"让时间陪你慢慢变富\"、\"七年就是一辈子\"、\"元认知\"、\"活在未来\"、\"复利\u002F长期主义\"、\"践行\"、\"痴迷改进\"、\"个人商业模式\u002F出售时间\"、\"睡后收入\"、\"定投\"、\"财富自由\"、\"操作系统升级\"、\"最少必要知识\"、\"北极星提示词\"、\"用 AI 该怎么学\u002F思考\" 等任一触发词,或当用户带着关于创业\u002F赚钱\u002F投资\u002F学习\u002F职业\u002F重大人生决策的困惑、希望被人用笑来式的「逻辑 + 大白话 + 类比 + 重新定义 + 践行导向」来点醒和指导时,自动进入李笑来教练模式。","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fxiaolai-methodology\u002FSKILL.md",[103],{"categoryNo":104,"categoryName":105,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000018","写作与文案",[107,108,109,110,111,112,113],"methodology","xiaolai","xiaolai methodology","朋友","投资","writing","收入",{"skillNo":115,"name":116,"nameZh":6,"description":117,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":118,"categories":119,"keywords":126,"publishedAt":49},"01M70P13NB9YP7ACJR1S861CDS","zread","Produce and consume a wiki-style knowledge base for a code repository via the `zread` CLI and its on-disk output under `.\u002F.zread\u002Fwiki\u002F`. Use this skill whenever the user wants to understand, onboard onto, explore, summarize, map, or get an overview of an unfamiliar codebase; asks for architecture docs, a project wiki, a repo walkthrough, module\u002Fpackage explanations, or \"what does this repo do\"; wants to generate, regenerate, resume, browse, or serve code documentation locally; or mentions zread \u002F zread.ai directly. Also use it proactively before diving into a large unknown repo — if `.\u002F.zread\u002Fwiki\u002Fcurrent` exists, read the generated pages instead of crawling source file-by-file; if it doesn't, consider offering to run `zread generate`. The trigger is the intent (understand a codebase through generated docs), not the literal word \"zread\".","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Fzread\u002FSKILL.md",[120,123],{"categoryNo":121,"categoryName":122,"taxonomyType":21,"taxonomyTypeDesc":22},"01JBSEEDCAT000000000000023","Skill与智能体开发",{"categoryNo":124,"categoryName":125,"taxonomyType":26,"taxonomyTypeDesc":27},"01JBSEEDCAT000000000000030","开发工程师",[116,127,128,129,130,131,132,133,134,135,136,137,138,29,139,140,141,142,143,144],"knowledge","wiki","explore","walkthrough","project","get","knowledge base","run","generate","intent","cli","map","project wiki","disk","architecture","code","unknown","generated",{"skillNo":146,"name":147,"nameZh":6,"description":148,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":149,"categories":150,"keywords":155,"publishedAt":49},"01M70P10S4SWMZQ8BJAFBFDRW3","youtube","Launch the YouTube Creator Agent to auto-generate videos.\nUse when: user types \u002Fyoutube, wants to create YouTube videos,\ngenerate video content, or upload to YouTube.\nKeywords: youtube, video, 视频, 创作视频, 发布视频","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Fyoutube\u002FSKILL.md",[151,152],{"categoryNo":121,"categoryName":122,"taxonomyType":21,"taxonomyTypeDesc":22},{"categoryNo":153,"categoryName":154,"taxonomyType":26,"taxonomyTypeDesc":27},"01JBSEEDCAT000000000000036","内容创作者",[147,156,157,158,159,160,161,162,135,163,164,165,166,34,167,168,169,170],"user","content","视频","creator","generate video","videos","launch","video content","create","upload","when","auto","types","Video","创作",{"skillNo":172,"name":173,"nameZh":6,"description":174,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":175,"categories":176,"keywords":178,"publishedAt":49},"01M70P0YE95D8BACZCGV8BK90K","youtube-script-sync","Sync, update, or optimize Tony's GetNote knowledge base `Youtube视频逐字稿` by turning each parent recording or first-person idea note into an idempotent child note containing a directly recordable YouTube long-video or Shorts script. Use when the user says “更新\u002F同步\u002F优化 Youtube视频逐字稿知识库”, or says “更新\u002F同步\u002F优化该知识库” while this knowledge base is the active context.","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Fyoutube-script-sync\u002FSKILL.md",[177],{"categoryNo":121,"categoryName":122,"taxonomyType":21,"taxonomyTypeDesc":22},[179,180,147,181,182,169,183,184,185,186,187,188,189,190,133,191,166,34,127,192],"sync","script","youtube script sync","recording","shorts","first","base","person","update","active","child","optimize","idempotent","long",{"skillNo":194,"name":195,"nameZh":6,"description":196,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":197,"categories":198,"keywords":203,"publishedAt":49},"01M70P0WMV5XT0EEC0N445PW07","writing-skills","How to write SKILL.md files that trigger reliably and teach effectively. Use when creating, improving, or reviewing Claude Code skills.","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Fxiaolai\u002Fnlpm\u002Fskills\u002Fnlpm\u002Fwriting-skills\u002FSKILL.md",[199,200,201,202],{"categoryNo":104,"categoryName":105,"taxonomyType":21,"taxonomyTypeDesc":22},{"categoryNo":121,"categoryName":122,"taxonomyType":21,"taxonomyTypeDesc":22},{"categoryNo":124,"categoryName":125,"taxonomyType":26,"taxonomyTypeDesc":27},{"categoryNo":153,"categoryName":154,"taxonomyType":26,"taxonomyTypeDesc":27},[204,112,205,206,207,208,142,166,34,209,210,211,212],"writing skills","how","teach","write skill","write","claude code skills","files","how to","trigger",{"skillNo":214,"name":215,"nameZh":6,"description":216,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":217,"categories":218,"keywords":221,"publishedAt":49},"01M70P0SJFR4YVJQBGMHKGSKXT","writing-rules","How to write .claude\u002Frules\u002F files that Claude actually follows. Use when creating, improving, or reviewing project rules.","https:\u002F\u002Fgithub.com\u002Fshengdabai\u002FTony-Claude-Code-Skills\u002Fblob\u002Fmain\u002Fskills\u002Fxiaolai\u002Fnlpm\u002Fskills\u002Fnlpm\u002Fwriting-rules\u002FSKILL.md",[219,220],{"categoryNo":104,"categoryName":105,"taxonomyType":21,"taxonomyTypeDesc":22},{"categoryNo":153,"categoryName":154,"taxonomyType":26,"taxonomyTypeDesc":27},[222,112,223,131,224,210,166,205,208,34,211],"Rules","writing rules","project rules"]