Source assessmentSupporting
Interplay between the Medical Devices Regulation (MDR) & In vitro Diagnostic Medical Devices Regulation (IVDR) and the Artificial Intelligence Act (AIA)
European AI Board governanceRegulatory/legal
Assessment outcome
total 2/4 (actionability 0 + authority 2); currency unscored, so pro-rated to 3.0/6
Total2/6
Actionability0/2
Authority2/2
Currency—
Authorship & scope
Attribution (G4 evidence)
No evidence recorded for this source.
Issuer authority (evidence)
No evidence recorded for this source.
Issuers, who it governs, legal force and content are on the full record.
Eligibility gates
G1 · Retrievablepass
Passed in screening.
G2 · AI nexuspass
Passed in screening.
G3 · Governance nexuspass
Passed in screening.
G4 · Attributablepass
Passed in screening.
G5 · In forcepass
Passed in screening.
Scored criteria
Actionability
0/2No rationale recorded.
Authority
2/2No rationale recorded.
The European Artificial Intelligence Board (the AI Board) is a key advisory body that was created by the AI Act
Currency
—No rationale recorded.
Classification
Coverage topicEuropean AI Board governance
PerspectiveRegulatory/legal
Lifecycle stageN/A cross-cutting
Layerboth
GranularityNot recorded