Applications and Challenges of Artificial Intelligence and Big Data in Drug Regulation

Artificial intelligence (AI) and big data are increasingly applied in drug regulation and have demonstrated significant potential worldwide. The U.S. Food and Drug Administration (FDA) has developed a relatively comprehensive approach through strategic frameworks, regulatory guidelines, and pilot programs. The European Medicines Agency (EMA) has promoted AI adoption via the Big Data Task Force, DARWIN EU^®, and a multi-annual work plan, while Japan, Canada, and other countries have also advanced relevant initiatives and strengthened international cooperation. In China, smart regulation has been incorporated into the "14th Five-Year Plan" and subsequent strategies, with progress in establishing national regulatory data platforms, pharmaceutical traceability systems, and pilot AI applications. Nevertheless, AI in drug regulation remains at an exploratory stage, facing challenges such as limited model reliability and interpretability, insufficient data standards and interoperability, regulatory gaps, and ethical as well as public trust concerns. Future progress will depend on strengthening regulatory standards, enhancing data governance, improving regulatory capacity, and deepening international collaboration to achieve more scientific, intelligent, and efficient drug regulation.