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US, European regulators set principles for ‘good AI practice’ in drug development

The U.S. Food and Drug Administration and the European Medicines Agency jointly issued principles for safe and responsible use of artificial intelligence in developing medicines, aiming to speed up innovation while safeguarding patients.

Jan 14 (Reuters) – The U.S. Food and Drug Administration and the European Medicines Agency jointly issued principles for safe and responsible use of artificial intelligence in developing medicines, aiming to speed up innovation while safeguarding pat… [1276 chars]

Source: Reuters | Published: 2026-01-14T16:32:54Z

Credit: Reuters

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