Skill UI

A comprehensive guide for achieving compliance with the EU MDR 2017/745. It covers crucial aspects including medical device classification (Annex VIII), developing technical documentation (Annex II/III), planning clinical evaluation (CER), and establishing post-market surveillance (PMS/PSUR) systems. Ideal for regulatory specialists preparing for Notified Body audits or needing to gap-check technical files.

A comprehensive guide for implementing ISO 14971:2019 risk management across the entire medical device lifecycle. Covers planning, hazard identification, risk analysis (FMEA, FTA), risk evaluation, risk control, and post-market surveillance. Essential for achieving regulatory compliance in medical device development.

This tool provides comprehensive integration for Reolink security cameras, supporting both RTSP streaming and HTTP API access. It allows users to discover cameras via ONVIF, capture live streams, take snapshots, and even capture motion-triggered video clips. It is ideal for developers building robust, networked surveillance or monitoring systems.

This utility enables multi-camera streaming by converting standard camera protocols (RTSP, RTMP, HTTP) into low-latency WebRTC streams using the go2rtc sidecar. It is essential for building real-time surveillance dashboards, live video monitoring systems, or integrating diverse IP cameras into a single web interface.

This skill provides high-performance, real-time object detection utilizing the Google Coral Edge TPU accelerator. It processes live camera frames to identify up to 80 COCO classes (e.g., person, car, dog). Optimized for native macOS and Linux deployment, it achieves extremely low latency (e.g., ~4ms at 320x320), making it ideal for embedded vision systems, surveillance, and low-latency monitoring applications.

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.