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Compliance isn't
a constraint.
It's a competitive advantage.
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It's a competitive advantage.
General-purpose AI models like GPT-4 and Claude face specific EU AI Act obligations distinct from the high-risk AI regime. This explainer breaks down what GPAI means, which models are covered, and what providers must do.
Traditional AI Act consulting audits cost €15,000–50,000 and take months. Dilaig generates the same four mandatory documents in under an hour. Here is what that difference means in practice for SMEs and startups.
Healthcare AI faces two overlapping regulatory regimes: the EU AI Act and MDR/IVDR. This guide explains both, how they interact, and what your team must do.
A practical breakdown of EU AI Act fines, enforcement bodies, and investigation triggers — so you know your real compliance risk and when it starts.
What the GPAI Code of Practice means for AI model providers: legal status, four obligation measures, the 10²⁵ FLOPs threshold, and signing implications.
A practical guide for high-risk AI providers on the two assessment paths, the step-by-step process, required documentation, and key August 2026 (postponed to 2 December 2027 under the AI Omnibus agreement) deadlines.
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