ConceptCE认证 / CE标志
CE
A mandatory product safety certification mark of the European Union, indicating that a product complies with the relevant EU directives and standards. It is an access requirement for products such as medical devices entering the European market.
Timeline (last 90 days)
Oct 23
Regulators such as the FDA and CE have begun requiring submission of subgroup performance analyses to ensure that AI tools are safe and effective across different populations.
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