Skill UI

Guides medical device teams through preparing ISO 13485:2016 Quality Management System documentation by combining gap analysis, requirements references, templates, and step-by-step creation workflows for manuals, procedures, and compliance artifacts.

This module is designed to document, track, and manage quality nonconformance issues found during manufacturing or process audits. It is essential for root cause analysis, implementing corrective and preventive actions (CAPA), and ensuring compliance with industry quality standards. Use it when recording deviations from specified requirements.

This tool performs comprehensive API inventory and discovery across an organization's environment. It identifies all API endpoints—including documented, undocumented, shadow, and deprecated APIs—by combining passive traffic analysis (HAR files), active scanning, DNS enumeration, and cloud resource auditing. It helps map the complete API attack surface, crucial for security assessments and compliance requirements like PCI-DSS and SOC2.

This module is designed to document, track, and manage quality nonconformance issues found during manufacturing or process audits. It is essential for root cause analysis, implementing corrective and preventive actions (CAPA), and ensuring compliance with industry quality standards. Use it when recording deviations from specified requirements.