Skill UI

This guide provides practical implementation steps for ensuring GDPR compliance in data processing, consent management, and privacy controls. Use this skill when developing systems that handle EU personal data, managing Data Subject Requests (DSRs), or designing privacy-first architectures to meet strict international data regulations.

Provides senior regulatory affairs guidance for HealthTech and MedTech firms, driving FDA 510(k)/De Novo/PMA submissions, CE marking, and multi-market access strategies while maintaining intelligence on evolving regulations.

This router bundles 15 specialized compliance skills crucial for HealthTech and MedTech organizations. It provides structured guidance across major global regulations, including ISO 13485 QMS, EU MDR, FDA submissions, GDPR, and the EU AI Act. Use this when a compliance request is complex and needs to be accurately directed to a specific technical skill area (e.g., risk management, CAPA, data security).

A comprehensive guide to implementing technical and organizational measures required by the General Data Protection Regulation (GDPR). This skill covers full lifecycle data protection, including Data Protection by Design, Data Protection Impact Assessments (DPIAs), managing data subject rights (e.g., right to erasure, portability), encryption, pseudonymization, and ensuring cross-border data transfer compliance.

AKF is the native metadata format specifically designed for tracking AI-generated or AI-modified content. It allows users to stamp files (including DOCX, PDF, images, and code) with detailed trust scores, source provenance, and compliance metadata. This tool is essential for professional workflows requiring strict auditing, compliance assurance, and verifiable data lineage, especially concerning regulations like the EU AI Act, HIPAA, and SOX.

A comprehensive toolkit for medical device manufacturers seeking ISO 13485 certification. This skill guides users through gap analysis, creating mandatory Quality Management System (QMS) documentation, and ensuring compliance with global medical device regulations (e.g., EU MDR, FDA QMSR). It provides templates, guidance, and structured processes for foundational QMS documents like Quality Manuals and CAPA procedures.

A practical coach designed to develop the four core EQ competencies: self-awareness, self-regulation, empathy, and social skills. Utilizing concepts from affective neuroscience and established frameworks, it guides users to identify precise emotions, understand triggers, manage difficult feelings non-reactively, and improve interpersonal relationships while accounting for cultural emotional norms.

An operational compliance tool for the EU AI Act (Regulation (EU) 2024/1689). It assists compliance teams with three critical decisions: classifying AI risk tiers (prohibited, high, limited, minimal), planning conformity assessment routes for high-risk systems (Module A vs. Module H), and tracking role-specific obligations for providers, deployers, and importers. Provides article-cited guidance for system intake and regulatory planning.

This skill provides regulator-grade feature attribution for complex trading signals (LSTM/Transformer). By constructing a feature-contribution graph and running single-entry PageRank, it identifies the top-K features that most drove a prediction. This is crucial for compliance with regulations like the EU AI Act and SEC Reg-AI, providing a robust, auditable audit trail for algorithmic trading systems.