Before a subject participates in testing in real world conditions under Art.60, freely given informed consent must be obtained after the subject has been duly informed, in concise, clear, relevant and understandable terms, of the nature and objectives of the testing and the possible inconvenience of participating; the conditions under which the testing will be conducted, including the expected duration of their participation; their rights and the guarantees regarding their participation, in particular the right to refuse and the right to withdraw at any time without any resulting detriment and without giving reasons; the arrangements for requesting the reversal or disregarding of the system's predictions, recommendations or decisions; and the Union-wide unique single identification number of the testing together with contact details for the provider or its legal representative. The consent must be dated and documented, and a copy given to the subject or their legal representative.
EU AI Act EUAI-Art.61 is one control. If you already hold one of the frameworks below, a reviewed crosswalk already says how much of EU AI Act your existing evidence covers. Hold ISO/IEC 42001:2023 and 17 of 43 EU AI Act controls already carry evidence.
Each report names every control your existing framework evidences, every one it does not, the reasoning behind each claim, and the claims that were argued against and rejected. 0 were rejected on the ISO/IEC 42001:2023 pair alone.
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.