NostraPharma
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EU AI Act – Compliance Checker

Which kind of entity is your organisation?

Selected entity: —

Do you (or a downstream deployer, distributor, or importer) make any of the following modifications to your system?

Modifications: none

Does your product integrate an AI system AND meet either of the following criteria?

E3: none

Does your AI system fall within any of the following high-risk categories? (Annex I, Section B)

HR1 (Annex I-B): none

Does your AI system fall within any of the following high-risk categories? (Annex I, Section A)

HR2 (Annex I-A): none

Is your product (or the product for which your AI system is a 'safety component') required to undergo a third-party conformity assessment under existing EU laws?(HR3)

HR3 (Sectoral third-party conformity): —

Does your AI system fall within any of the Annex III high-risk use cases?

HR4 (Annex III): none

Does your AI system pose a significant risk to health, safety or fundamental rights of any person? (HR5)

HR5: (no answer selected)

Is the AI system a safety component of a regulated product? (HR6)

HR6 (Safety component): No

Do you meet any of the following criteria? (S1)

S1 (Scope): none

Does your AI model meet any of the following systemic-risk criteria? (R1)

R1 (GPAI/systemic): none

Does your system or use case fall within any exclusion categories? (R2)

R2 (Exclusions): none

Does your system perform any prohibited practices? (R3)

R3 (Prohibited): none

Does your system trigger any transparency obligations? (R4)

R4 (Transparency): none

Are you a body governed by public law, or a private entity providing public services? — Fundamental Rights Impact Assessment (FRIA) (R5)

R5 (FRIA): —

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