Skill UI

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.

Provides a comprehensive monitoring solution for the Perplexity Sonar API. It tracks critical performance metrics, including latency (p95), cost per query, error rates, and citation quality. This skill is essential for implementing production monitoring dashboards, configuring proactive alerts (e.g., high latency, zero citations), and ensuring the API's stability and high-quality output in real-world applications.

This skill provides comprehensive expertise for senior database administrators to optimize and manage PostgreSQL databases at an advanced level. Use it for deep query analysis via EXPLAIN ANALYZE, implementing advanced features like JSONB indexing, configuring streaming or logical replication, and maintaining database health through VACUUM tuning and monitoring pg_stat views. Ideal for building highly available, high-performance, and resilient system architectures.

Monitor the operational health of PostHog integrations by tracking critical metrics. This skill checks event ingestion rates, feature flag evaluation latency, and monitors billing volume consumption. It also provides rules for Prometheus/Grafana alerting, ensuring data pipelines remain stable and alerting on potential performance bottlenecks or exceeding API limits.

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 skill provides comprehensive methodologies for capturing, analyzing, and documenting network protocols. It is crucial for security researchers, developers ensuring interoperability, and engineers debugging complex network communications by understanding the underlying data exchange mechanisms.

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.

This skill provides comprehensive guidance and tools for end-to-end software release management. It automates critical tasks such as generating changelogs from conventional commits, determining semantic version bumps (Major/Minor/Patch), assessing release readiness, and planning complex deployment workflows (e.g., Git Flow). Ideal for teams adopting robust DevOps practices.

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.