EU Report Shows Surge In Industry AI Use – But Are Regulators Ready?

- A European Medicines Agency (EMA) report reveals a surge in AI adoption by pharmaceutical companies across the entire drug development lifecycle.
- Industry applications currently range from optimizing clinical trial site selection to the automated drafting of complex regulatory documents.
- The report warns that significant "gaps remain" regarding the AI tools used for regulatory assessments, questioning if regulators are equipped to keep pace.
- This discrepancy highlights a growing tension between rapid private-sector innovation and the slower evolution of public oversight frameworks for drug safety.
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