On January 7, 2025, the MDCG 2023-3, a guidance document from the Medical Device Coordination Group (MDCG) of the European Union, was updated to Revision
The United States Food and Drug Administration (FDA) released a draft guidance document on January 6, 2025, outlining its recommendations to facilitate the development and
Today marks a milestone for the EU as the AI Act enters into force after three years of development. The EU leads as the first to establish a robust AI regulatory framework. With the countdown for implementation beginning, let’s explore the timelines ahead.
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