Skill UI

This comprehensive runbook provides step-by-step procedures for managing MaintainX integration failures. It guides users through severity classification, immediate triage, root cause analysis, and mitigation strategies (such as key rotation or request buffering). The playbook ensures systematic incident response, verification of recovery, and proper post-mortem documentation for rapid system restoration.

A comprehensive, step-by-step guide for security professionals to perform deep-dive malware analysis. It covers methodologies for static analysis (disassemblers, imports), dynamic execution (sandboxing, monitoring), identifying Indicators of Compromise (IOCs), and structuring professional threat reports. Essential for incident response and threat intelligence.

This skill guides the implementation of comprehensive, real-time monitoring for APIs. It covers collecting key metrics (latency, error rates, request rate), setting up health and readiness endpoints, building detailed Grafana dashboards, and implementing SLO-based alerting (following the RED method). Use this when you need to ensure API reliability, high availability, and performance in a production environment.

Designs comprehensive, production-ready observability strategies by integrating metrics, logs, and traces. This tool guides the setup of SLI/SLO frameworks, optimizes noisy alerting configurations, and generates detailed dashboards, ensuring deep visibility into service health and performance.

This skill specializes in implementing Service Level Objectives (SLOs) and Service Level Indicators (SLIs) to enforce reliability standards. It guides users in designing comprehensive SLO frameworks, calculating error budgets, and building robust monitoring systems. Use this when you need to establish data-driven reliability targets, balance feature velocity with technical health, and align service performance directly with core business objectives.

This comprehensive playbook provides effective patterns and structured templates for managing on-call shift transitions. It guides engineers on documenting active incidents, ongoing investigations, recent system changes, and upcoming maintenance events. The goal is to ensure seamless context transfer, maintaining continuity and reliable incident response across different shifts.

A comprehensive guide covering the complete setup of Prometheus, including metric collection strategies, advanced scrape configuration (static, file-based, Kubernetes), defining recording rules, and integrating with AlertManager and Grafana. Use this skill to establish robust monitoring for applications and infrastructure.

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, step-by-step guide for deploying applications on Replit to production environments. It covers crucial best practices, including configuring deployment settings, managing environment secrets, implementing robust health checks, handling global errors, setting up custom domains, and defining rollback strategies. Essential for developers preparing an app for a live launch or scaling up.

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.