CLUSTER / THE DECISION MAP
EU database, registration and post-market monitoring.
Registration, the EU database, post-market monitoring and serious incident reporting.
IN THIS CLUSTER
12 guides.
What Is the EU Database for High-Risk AI Systems?
An overview of the EU database, registration and post-market monitoring: who registers, what the database contains, what is public, and how registration connects to monitoring and incident reporting.
Read guide ↗CLUSTER ARTICLEWhat Does Article 71 Say About the EU Database?
Article 71 in outline: how the EU database is set up, what information it contains, who enters it, and the public access and restricted-section rules that govern it.
Read guide ↗CLUSTER ARTICLEWhat Must Providers Register Under Article 49?
Provider registration under Article 49: when registration must happen, what it covers for Annex III systems, the role of authorised representatives, and how it links to classification.
Read guide ↗CLUSTER ARTICLEWhich Deployers Must Register Their Use of a High-Risk System?
Deployer registration under Article 49(3): which public authorities and Union bodies must register, what they register, and how deployer registration differs from provider registration.
Read guide ↗CLUSTER ARTICLEMust a System Concluded Not to Be High-Risk Still Be Registered?
Registration after an Article 6(3) conclusion: what a provider must document, what must be registered under Article 49(2), and how the simplified registration works after Regulation (EU) 2026/1744.
Read guide ↗CLUSTER ARTICLEWhat Is Public and What Is Restricted in the EU Database?
Public and restricted access to the EU database: the Article 49(4) secure section, national registration, Article 60 testing information, and how to identify the right access category before submitting.
Read guide ↗CLUSTER ARTICLEWhat Information Must Be Entered Under Annex VIII?
Annex VIII in outline: the provider, system and deployer information entered in the EU database, how the sections divide, and how to prepare an accurate entry without adding material beyond the Annex.
Read guide ↗CLUSTER ARTICLEWhen Must Registration Happen, and When Must an Entry Be Updated?
Registration timing and updates: the before-market rule, what changes trigger a new or corrected entry, version control, and how to keep registration aligned with documentation and monitoring.
Read guide ↗CLUSTER ARTICLEWhat Is Post-Market Monitoring Under Article 72?
Post-market monitoring for high-risk AI systems: the provider's monitoring system and plan, the data it must collect and analyse, and how findings feed back into risk management and corrective action.
Read guide ↗CLUSTER ARTICLEHow Must Serious Incidents Be Reported Under Article 73?
Serious incident reporting for high-risk AI systems: what counts as a serious incident, who reports, to whom, within which period, and how reporting connects to post-market monitoring and corrective action.
Read guide ↗CLUSTER ARTICLEHow Does Testing in Real World Conditions Work Under Article 60?
Testing in real world conditions under Article 60: when testing is allowed, the testing plan and authority approval, Annex IX registration, safeguards for test subjects, and the link to sandboxes.
Read guide ↗CLUSTER ARTICLEHow Should Record-Keeping Link Registration to Compliance Evidence?
Record-keeping that connects registration, technical documentation, logs, quality management and post-market monitoring into one traceable evidence chain for each high-risk system version.
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