Spec To Code Compliance Checker

Investigate root causes and manage CAPAs (Corrective and Preventive Actions) for compliance deviations. Covers investigation method selection (5-Why, fishbone, fault tree), structured root cause analysis, corrective vs preventive action design, effectiveness verification, and trend analysis. Use when an audit finding requires a CAPA, when a deviation or incident occurs in a validated system, when a regulatory observation needs a formal response, when a data integrity anomaly requires investigation, or when recurring issues suggest a systemic root cause.

Drift detection + baseline integrity guard for agent workspace files with automatic alerting support

Audit project dependencies for version staleness, security vulnerabilities, and compatibility issues. Covers lock file analysis, upgrade path planning, and breaking change assessment. Use before a release to ensure dependencies are current and secure, during periodic maintenance reviews, after receiving a security advisory, when upgrading to a new language version, before submitting to CRAN or npm, or when inheriting a project to assess its dependency health.

Revisa el diff de la rama actual frente a develop en proyectos Drupal 11 siguiendo la metodología Codex (lógica de negocio, edge cases de hooks/queries, seguridad, performance, completitud). Genera un informe .md en la carpeta del IDE detectado (.antigravity/, .cursor/, .vscode/ o docs/) con hallazgos por severidad y soluciones accionables. Usar cuando el usuario pida "Revisión diff develop", "revisión diff develop", "diff develop", "revisar diff", "codex diff" o expresiones similares con intención de auditar cambios contra develop. Triggers: diff develop, codex diff, revisión diff, lint diff develop, auditar diff.

ISO 13485 internal audit expertise for medical device QMS. Covers audit planning, execution, nonconformity classification, and CAPA verification. Use for internal audit planning, audit execution, finding classification, external audit preparation, or audit program management.

Prepare an organisation for regulatory inspection by assessing readiness against agency-specific focus areas (FDA, EMA, MHRA). Covers warning letter and 483 theme analysis, mock inspection protocols, document bundle preparation, inspection logistics, and response template creation. Use when a regulatory inspection has been announced or is anticipated, when a periodic self-assessment is due, when new systems have been implemented since the last inspection, or after a significant audit finding that may attract regulatory attention.