ios-qa
ios-qa
Live-device iOS QA for SwiftUI apps. (gstack)
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ruview-hardware-setup
ruview-hardware-setup
ESP32-S3 / ESP32-C6 firmware build, flash, WiFi provisioning, and serial monitoring for RuView CSI sensing nodes. Use when setting up physical hardware, reflashing a node, or debugging a device that isn't streaming CSI.
favicons
favicons
Use when reviewing templates, rendered HTML, or shared components related to Implement favicons for all devices. Validate the final browser-facing markup, not just the source framework abstraction.
mobile-testing
mobile-testing
Use when reviewing CI coverage, automated checks, or test strategy related to Test on real mobile devices and viewports. Focus on whether the rule is continuously verified, not just documented.
scheduler-yield
scheduler-yield
Use when reviewing JavaScript that performs synchronous loops over large datasets, recursive tree traversals, or bulk DOM updates that may exceed 50 ms on mid-range devices.
iso-standards-readiness
iso-standards-readiness
Prepares and structurally reviews readiness evidence for ISO management-system and laboratory-competence standards - ISO 13485 medical device QMS, ISO 14971 device risk management, ISO/IEC 17025 testing and calibration laboratories, and ISO 15189 medical laboratories. Use when organizing declared scope, controlled documents, risk-management files, scope of …
neurokit2
neurokit2
Builds and audits reproducible NeuroKit2 research workflows for physiological time-series preprocessing, event/interval analysis, multimodal alignment, variability, and complexity. Use when code imports neurokit2 or needs its current APIs, schemas, and method-aware validation—not for diagnosis or device validation.
pylabrobot
pylabrobot
Develops and reviews PyLabRobot lab-automation resources, liquid-handling plans, offline simulations, and supported-device integrations. Supports PyLabRobot protocols and API questions; keep physical execution behind an explicit operator safety gate.
appium-skill
appium-skill
Generates production-grade Appium mobile automation scripts for Android and iOS in Java, Python, or JavaScript. Supports real device and emulator testing locally and on TestMu AI cloud with 100+ real devices.
apple-notes-search
apple-notes-search
Semantic + keyword search and connection-discovery across the user's own Apple Notes via the apple-notes MCP server. Use when the user wants to find, recall, or synthesize something from their notes, or surface non-obvious bridges/related notes. macOS, on-device.
cloudflare-zero-trust
cloudflare-zero-trust
Protect internal apps with Cloudflare Access, device posture, and Zero Trust policies.
fda-medtech-compliance-auditor
fda-medtech-compliance-auditor
Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation.
mdm-device-management
mdm-device-management
Manage and secure company devices with MDM solutions
premium-3d-website
premium-3d-website
Guidelines for building premium 3D websites, focusing on custom WebGL shaders, post-processing, physics-based interactions, smooth animations, preloaders, and device optimization.
exploring-live-traffic
exploring-live-traffic
Inspects PostHog Web analytics Live tab data — current users online, last-30-minutes pageviews, top pages, referrers, devices, browsers, countries, bot traffic, and the per-minute bot/users charts. Use when the user asks "who is on my site right now?", "what is happening live?", "what bots are crawling me?", asks about the "live tab" / "live dashboard", wan…
capa-officer
capa-officer
CAPA system management for medical device QMS. Covers root cause analysis, corrective action planning, effectiveness verification, and CAPA metrics. Use when running CAPA investigations, 5-Why analysis, fishbone diagrams, root cause determination, corrective action tracking, effectiveness verification, or CAPA program optimization.
fda-consultant-specialist
fda-consultant-specialist
FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QMSR (21 CFR 820, which incorporates ISO 13485:2016 by reference since 2026-02-02; formerly QSR) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QMSR, QSR, ISO 13485 for FDA, premarket, p…
mdr-745-specialist
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, Art. 86 PSUR schedules, and EUDAMED integration. Use when classifying a medical device under MDR, building or g…
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Direct from traceable public skill sources
An independently imported catalog with original authors, licenses and source links. Classification is not a security audit.
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