Skill UI

This comprehensive guide establishes the standards for a modern, minimalist, and highly functional design system. It defines foundational elements like typography, color tokens, and spacing scales, while strictly adhering to WCAG 2.2 AA accessibility. It provides structured workflows, detailed component rules, and quality gates for both designers and engineers to ensure consistent, usable, and aesthetically pleasing product experiences.

This skill provides expert guidance on creating comprehensive, implementation-ready design system documentation. It covers visual foundations (color, typography, spacing), component anatomy, interaction states, and rigorous accessibility standards (WCAG 2.2 AA). Use it to ensure product consistency and quality across engineering and design teams.

This comprehensive guide provides expert, implementation-ready guidelines for building narrative-driven digital experiences. It covers foundational elements like visual style, typography, color tokens, and spacing, alongside strict component rules and accessibility standards (WCAG 2.2 AA). Use it to transform functional interfaces into emotionally resonant and memorable user journeys.

A comprehensive, implementation-ready guide for building editorial interfaces. This system defines foundational tokens, typography (DM Serif Display), color palettes, and accessibility standards (WCAG 2.2 AA) to create clean, readable, and aesthetically rich long-form content layouts, perfect for blogs and storytelling platforms.

This guide teaches you how to function as an expert design-system guideline author for the 'Vibrant' brand. It provides comprehensive, implementation-ready documentation covering foundational tokens (color, typography, spacing), detailed component rules (states, variants, interactions), and adherence to WCAG 2.2 AA accessibility standards. The output is structured, actionable, and includes quality assurance checklists for both designers and engineers.

Act as an expert guide author specializing in the Vintage design aesthetic (1950s–1990s). This skill provides comprehensive, implementation-ready guidelines for creating design systems, covering visual tokens, component anatomy, accessibility standards (WCAG 2.2 AA), and strict writing rules. It ensures output is structured, opinionated, and highly practical for engineers and designers.

A meta-orchestrator designed for compliance teams to manage complex, multi-jurisdictional compliance programs. It automatically selects applicable regulatory frameworks (e.g., ISO 27001, GDPR, EU AI Act, HIPAA), computes control overlap across standards, simulates mock audits, and consolidates evidence into a unified reuse map. Ideal for planning annual audits or achieving multi-certification.

This tool simulates a highly critical compliance officer, forcing rigorous scrutiny on any multi-framework compliance program. It addresses six critical areas: scope definition, evidence overlap, ownership accountability, audit planning, mock audit simulation, and management review cadence. Use it before adopting new standards (like ISO or HIPAA), planning annual audits, or preparing for major certifications to systematically identify gaps and risks.

A comprehensive simulation tool designed to pressure-test medical device manufacturers' Quality System Regulation (QSR) compliance against FDA standards (21 CFR 820). It covers six critical areas: complaint handling, process validation, device history records (DHRs), CAPAs, labeling, and handling of Form 483 observations. Essential for pre-inspection readiness, internal audits, and regulatory submission planning.

This skill acts as an expert author for creating comprehensive, implementation-ready design system guidelines. It covers foundational elements, including brand identity, color tokens, typography scales, and spacing rules. It mandates structured documentation, component state definitions (default, hover, error, etc.), and strict adherence to WCAG accessibility standards, ensuring consistency and usability across all digital products.

This tool performs a rigorous, simulated Quality Management System (QMS) audit based on ISO 13485 standards for medical devices. It forces interrogation on critical areas, including Design History Files (DHF), CAPA effectiveness, process validation, risk management (ISO 14971), and post-market surveillance (MDR/FDA QSR). Use it before major audits, commercial launches, or regulatory submissions to identify compliance gaps.

This skill simulates a comprehensive auditor pressure test for any Information Security Management System (ISMS) against ISO 27001 standards. It forces interrogation on six critical areas—including scope, risk management, access control, and incident response—ensuring compliance and readiness before internal audits, Stage 1 certification, or surveillance audits.