post-market-monitor

Post-market surveillance monitors AI systems for compliance with Article 72 of the EU AI Act by tracking performance, user feedback, incidents, and serious events to ensure continued regulatory adherence.

Post-market surveillance for AI governance is the ongoing monitoring of deployed AI systems to ensure safety and compliance, required after an AI system launches to track incidents and regulatory adherence.

Assess compliance with Article 72 by evaluating your AI system against specific regulatory requirements, implementing controls, documenting performance, and establishing ongoing review processes.

Yes, you can track adverse events and monitor performance for AI-powered medical tools to ensure they remain compliant with post-market surveillance regulations after deployment.

AI risk management documentation requires tracking system performance, logging user feedback, recording incidents and serious events, and maintaining ongoing compliance assessment records.

Post-market monitoring focuses on tracking performance and incidents but requires continuous implementation of controls and documentation to maintain compliance, meaning it is an ongoing constraint rather than a one-time assessment.