ReddRadar
Topic: prompt-engineering
2,538 skills in this topic.
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gdpr-dsgvo-expert
GDPR and German DSGVO compliance automation. Scans codebases for privacy risks, generates DPIA documentation, tracks data subject rights requests. Use for GDPR compliance assessments, privacy audits, data protection planning, DPIA generation, and data subject rights management.
alirezarezvani/claude-skills 8,805
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information-security-manager-iso27001
ISO 27001 ISMS implementation and cybersecurity governance for HealthTech and MedTech companies. Use for ISMS design, security risk assessment, control implementation, ISO 27001 certification, security audits, incident response, and compliance verification. Covers ISO 27001, ISO 27002, healthcare security, and medical device cybersecurity.
alirezarezvani/claude-skills 8,805
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isms-audit-expert
Information Security Management System (ISMS) audit expert for ISO 27001 compliance verification, security control assessment, and certification support. Use when the user mentions ISO 27001, ISMS audit, Annex A controls, Statement of Applicability (SOA), gap analysis, nonconformity management, internal audit, surveillance audit, or security certification preparation. Helps review control implementation evidence, document audit findings, classify nonconformities, generate risk-based audit plans, map controls to Annex A requirements, prepare Stage 1 and Stage 2 audit documentation, and support corrective action workflows.
alirezarezvani/claude-skills 8,805
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mdr-745-specialist
EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, and EUDAMED integration.
alirezarezvani/claude-skills 8,805
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qms-audit-expert
ISO 13485 internal audit expertise for medical device QMS. Covers audit planning, execution, nonconformity classification, and CAPA verification. Use for internal audit planning, audit execution, finding classification, external audit preparation, or audit program management.
alirezarezvani/claude-skills 8,805
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quality-documentation-manager
Document control system management for medical device QMS. Covers document numbering, version control, change management, and 21 CFR Part 11 compliance. Use for document control procedures, change control workflow, document numbering, version management, electronic signature compliance, or regulatory documentation review.
alirezarezvani/claude-skills 8,805
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quality-manager-qmr
Senior Quality Manager Responsible Person (QMR) for HealthTech and MedTech companies. Provides quality system governance, management review leadership, regulatory compliance oversight, and quality performance monitoring per ISO 13485 Clause 5.5.2.
alirezarezvani/claude-skills 8,805
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quality-manager-qms-iso13485
ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support. Use when working with medical device quality systems, preparing for ISO 13485 audits, managing regulatory compliance documentation, setting up corrective actions, or building audit preparation programs. Useful for quality management, audit preparation, regulatory compliance, medical device documentation, and corrective action workflows.
alirezarezvani/claude-skills 8,805
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regulatory-affairs-head
Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathways for new medical devices; drafts responses to FDA deficiency letters and Notified Body queries; develops CE marking technical documentation under EU MDR 2017/745; coordinates multi-market approval strategies across FDA, EU, Health Canada, PMDA, and NMPA; and maintains regulatory intelligence on evolving standards. Use when users need to plan or execute FDA submissions, navigate 510(k) or PMA approval processes, achieve CE marking, prepare pre-submission meeting materials, write regulatory strategy documents, respond to agency queries, or manage compliance documentation for medical device market access.
alirezarezvani/claude-skills 8,805
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risk-management-specialist
Medical device risk management specialist implementing ISO 14971 throughout product lifecycle. Provides risk analysis, risk evaluation, risk control, and post-production information analysis. Use when user mentions risk management, ISO 14971, risk analysis, FMEA, fault tree analysis, hazard identification, risk control, risk matrix, benefit-risk analysis, residual risk, risk acceptability, or post-market risk.
alirezarezvani/claude-skills 8,805
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soc2-compliance
Use when the user asks to prepare for SOC 2 audits, map Trust Service Criteria, build control matrices, collect audit evidence, perform gap analysis, or assess SOC 2 Type I vs Type II readiness.
alirezarezvani/claude-skills 8,805
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agent-detector
CRITICAL: MUST run for EVERY message. Detects agent, complexity, AND model automatically. Always runs FIRST.
nguyenthienthanh/aura-frog 14
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angular-expert
Angular/TypeScript frontend expert. PROACTIVELY use when working with Angular, RxJS, NgRx. Triggers: angular, ngrx, rxjs, component.ts
nguyenthienthanh/aura-frog 14
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api-designer
Design consistent, RESTful APIs with proper versioning, documentation, and error handling.
nguyenthienthanh/aura-frog 14
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bugfix-quick
Fast bug fixes with TDD. Lightweight: understand → test → fix → verify.
nguyenthienthanh/aura-frog 14
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code-reviewer
6-aspect structured code review. Checks security, types, error handling, tests, quality, simplification.
nguyenthienthanh/aura-frog 14
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code-simplifier
Detect and simplify overly complex code. Apply KISS principle - less is more.
nguyenthienthanh/aura-frog 14
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debugging
Systematic debugging with root cause investigation. NO fixes without understanding cause first.
nguyenthienthanh/aura-frog 14
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design-expert
UI/UX design expertise - component design, design systems, responsive design, Figma analysis
nguyenthienthanh/aura-frog 14
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design-system-library
Design system selection and implementation helper. Detects and recommends UI libraries (MUI, Tailwind, shadcn/ui, etc.) based on project context.
nguyenthienthanh/aura-frog 14
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dev-expert
Development patterns for React, Vue, Laravel, Next.js, React Native - state management, forms, API integration
nguyenthienthanh/aura-frog 14
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documentation
Create Architecture Decision Records (ADRs) and Runbooks for operational documentation.
nguyenthienthanh/aura-frog 14
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flutter-expert
Flutter/Dart mobile expert. PROACTIVELY use when working with Flutter, Dart, mobile apps. Triggers: flutter, dart, widget, bloc, riverpod
nguyenthienthanh/aura-frog 14
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framework-expert
Unified framework expertise bundle. Lazy-loads relevant framework patterns (React, Vue, Angular, Next.js, Node.js, Python, Laravel, Go, Flutter, Godot) based on detected tech stack.
nguyenthienthanh/aura-frog 14