Skill UI

This advanced skill details dual-use security techniques for analyzing protected binaries, conducting malware analysis, and performing authorized penetration testing. It strictly mandates that users confirm explicit written authorization, adhere to defined scope, and ensure legal compliance (e.g., CFAA, DMCA). Use cases include CTF competitions, academic research, and internal security auditing, emphasizing defensive recommendations and evidence preservation.

This advanced skill details dual-use security techniques for analyzing protected binaries, conducting malware analysis, and performing authorized penetration testing. It strictly mandates that users confirm explicit written authorization, adhere to defined scope, and ensure legal compliance (e.g., CFAA, DMCA). Use cases include CTF competitions, academic research, and internal security auditing, emphasizing defensive recommendations and evidence preservation.

This skill automates the validation of AWS environments against critical industry compliance benchmarks. It performs detailed checks for CIS AWS Foundations, PCI-DSS, HIPAA, and SOC 2 standards, covering key areas like Identity and Access Management (IAM), logging, data protection, and network security. Essential for preparing for regulatory audits and maintaining continuous secure operations.

Automate the rotation of sensitive credentials, including RDS database passwords, API keys, and OAuth tokens, using AWS Secrets Manager and Lambda. This skill ensures secure credential lifecycle management, helping maintain system security and compliance by automatically updating credentials for various AWS and third-party services.

This comprehensive skill provides a security posture assessment for AWS environments. It uses AWS CLI commands to audit critical security areas, including IAM policy review, network security groups, data encryption status (EBS, S3, RDS), and logging mechanisms (CloudTrail, VPC Flow Logs). Use this to proactively identify misconfigurations and ensure adherence to security best practices and compliance standards.

Comprehensive guidance for medical device manufacturers navigating complex FDA regulatory requirements. Covers device classification, submission pathways (510(k), PMA, De Novo), Quality Management System Regulation (QMSR/ISO 13485), HIPAA compliance, and cybersecurity best practices. Use this when determining the correct regulatory route for a new or modified device.

This guide details setting up enterprise-grade access control for Langfuse. Learn how to configure role-based permissions (Owner, Admin, Member), implement scoped API keys, integrate SSO (SAML/OIDC), and set up comprehensive audit logging. It is essential for managing multi-team isolation and ensuring compliance in production environments.

This skill empowers users to manage and monitor critical SSL/TLS certificates using the built-in certificate manager. It provides capabilities to check certificate expiration dates, automate the renewal process for expired credentials, and list all installed certificates. It is essential for system administrators and developers maintaining secure, uninterrupted network connections and ensuring compliance.

This comprehensive guide provides expertise in conducting ISO 13485 internal audits for medical device Quality Management Systems (QMS). It covers the full audit lifecycle, including risk-based planning, systematic evidence collection, classifying nonconformities (Major/Minor), and managing CAPA verification to ensure regulatory compliance and continuous improvement.

A comprehensive guide for designing and managing document control systems for ISO 13485-compliant Quality Management Systems (QMS), specifically tailored for the medical device industry. This resource covers document numbering, version control, change management workflows, approval processes, and ensures compliance with rigorous standards like 21 CFR Part 11, including electronic signatures and audit trails.

This guide defines the role and responsibilities of a Senior Quality Manager Responsible Person (QMR) for highly regulated MedTech and HealthTech environments. It covers essential functions under ISO 13485, including leading management reviews, establishing quality objectives, monitoring performance KPIs, and maintaining strict regulatory compliance oversight. Use this resource when developing a Quality Management System (QMS) or managing regulatory accountability.

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.