Článek 17
Quality management system
Vysoké rizikoPoužitelné od 2. srpna 2026
Týká se: Poskytovatel
Providers of high-risk AI systems must put in place a documented quality management system covering strategy, procedures, and responsibilities for regulatory compliance.
Klíčové body
- Written policies, procedures, and instructions covering the full lifecycle
- Design control, development, verification, and testing procedures
- Data management and risk management procedures
- Post-market monitoring and serious-incident reporting arrangements
- Accountability framework covering management and staff responsibilities
Související pojmy
Tato stránka je srozumitelné shrnutí pro orientaci. Nejde o právní poradenství — závazný je text nařízení (EU) 2024/1689.