Skill UI

Guides medical device teams through preparing ISO 13485:2016 Quality Management System documentation by combining gap analysis, requirements references, templates, and step-by-step creation workflows for manuals, procedures, and compliance artifacts.

A rigorous, multi-phase auditing skill designed for blockchain protocols. It verifies whether the implemented smart contract code strictly adheres to the detailed specifications provided in whitepapers, design documents, or technical specifications. It performs exhaustive, line-by-line semantic analysis to identify gaps, inconsistencies, and deviations across logic, invariants, and security guarantees, making it essential for formal compliance checking in decentralized systems.

This skill guides the progressive adoption of the CISA Zero Trust Maturity Model (ZTMM) v2.0. It provides a comprehensive, structured roadmap for assessing and improving security architecture across five critical pillars: Identity, Devices, Networks, Applications, and Data. Learn to perform gap analysis and implement advanced controls needed to achieve optimal zero trust compliance.

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.

Generates a comprehensive, structured, and blameless incident postmortem document. This skill is designed for Root Cause Analysis (RCA), P1/P2 incident reviews, and outage reports, ensuring the focus remains on systemic gaps and preventative action items rather than individual blame. It guides the user through gathering all necessary details, from the timeline and impact to defining concrete action owners and due dates.