Skill UI

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 expert skill performs non-intrusive static analysis to thoroughly audit AI skills and bundles. It identifies malicious patterns, data leaks, system stability risks, and obfuscated payloads across major operating systems (Windows, macOS, Linux/Unix) and mobile platforms (Android/iOS). Use it when verifying skill legitimacy or performing deep cross-platform security reviews.

This guide details the comprehensive implementation of privileged session monitoring and recording using Privileged Access Management (PAM) solutions, such as CyberArk PSM. It covers essential steps including architectural routing, configuring keystroke logging, real-time risk analysis, and establishing secure, tamper-proof audit trails for critical administrative access (RDP, SSH, Databases). Essential for meeting strict compliance standards like SOX, HIPAA, and PCI-DSS.