Skill UI

This guide outlines security best practices for managing Bright Data zone credentials, API tokens, and webhooks. It covers crucial steps like credential inventory, environment variable security, zone isolation across environments, scheduled credential rotation, and implementing pre-commit hooks to prevent sensitive data leakage, maximizing data security and compliance.

Manages the complete data lifecycle within ClickHouse. Includes setting Time-To-Live (TTL) policies for automatic data expiration, implementing GDPR/CCPA compliant deletion, PII masking, partition management, and building comprehensive audit trails. Essential for robust data governance and compliance.

This comprehensive checklist guides developers through ensuring that Fathom API integrations are robust, secure, and fully compliant for production use. It covers critical areas including secrets management, rate limiting, webhook verification, advanced error handling (like circuit breakers), PII compliance, and comprehensive monitoring setup, ensuring reliable meeting data pipelines.

A comprehensive checklist designed to validate that an Oracle Cloud Infrastructure (OCI) environment meets rigorous production-grade standards. This tool automates checks for critical security controls, including compartment isolation, backup policy enforcement, NSG/security list auditing, API key rotation status, encryption verification, and compliance monitoring via Cloud Guard. Use it when preparing an OCI environment for mission-critical workloads or conducting a formal security audit.

A comprehensive guide detailing how to establish robust monitoring for Qdrant. Covers setting up Prometheus metrics scraping, implementing Liveness and Readiness probes for Kubernetes, configuring alerts, and centralizing logs. It provides specific instructions for both self-hosted and Hybrid Cloud environments, ensuring full operational visibility and compliance.

A comprehensive tool designed to pressure-test US medical device Quality System Regulation (QSR) compliance (21 CFR 820). It generates a readiness report by interrogating six critical areas—including complaints, CAPAs, and process validation—essential for internal audits, pre-FDA inspections, or responding to Form 483 observations. It ensures alignment with both FDA requirements and ISO 13485 standards.