All Skills

Review UI code for Web Interface Guidelines compliance. Use when asked to "review my UI", "check accessibility", "audit design", "review UX", or "check my site against best practices".

Fetch and extract readable content from web pages. Use for lightweight page access without browser automation.

Automates browser interactions for web testing, form filling, screenshots, and data extraction. Use when the user needs to navigate websites, interact with web pages, fill forms, take screenshots, or extract information from web pages.

A comprehensive and well-structured test automation strategy skill providing clear guidance on pyramid principles, patterns, CI/CD integration, and flaky test management with practical examples.

Automates browser interactions for web testing, form filling, screenshots, and data extraction. Use when the user needs to navigate websites, interact with web pages, fill forms, take screenshots, test web applications, or extract information from web pages.

This skill provides a detailed reference for writing Obsidian Flavored Markdown, covering wikilinks, callouts, properties, embeds, and other Obsidian-specific syntax. It serves as a quick lookup guide for users working with .md files in Obsidian, ensuring correct formatting and linking.

Toolkit for styling artifacts with a theme. These artifacts can be slides, docs, reportings, HTML landing pages, etc. There are 10 pre-set themes with colors/fonts that you can apply to any artifact that has been creating, or can generate a new theme on-the-fly.

Provides comprehensive guidance for using Plotly, a Python library for creating interactive visualizations. Covers both high-level Plotly Express and low-level Graph Objects APIs, with clear examples for common workflows like scientific plotting, statistical analysis, and dashboard creation. Includes practical advice on installation, export options, and integration with Dash.

Constant-time testing detects timing side channels in cryptographic code. Use when auditing crypto implementations for timing vulnerabilities.

Provides a structured template and methodology for creating SEO content briefs. Guides users through keyword research, SERP analysis, and outlining with specific requirements for writers. Includes checklists for quality control and E-E-A-T compliance.

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.

When the user wants to write, rewrite, or improve marketing copy for any page — including homepage, landing pages, pricing pages, feature pages, about pages, or product pages. Also use when the user says "write copy for," "improve this copy," "rewrite this page," "marketing copy," "headline help," or "CTA copy." For email copy, see email-sequence. For popup copy, see popup-cro.