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Boccuti V, Perrone A, DIntrono A, Campobasso A, Sangineto M, Sabb C

Literature search A comprehensive literature search was conducted in May 2025 across PubMed, Embase via OVID and the Cochrane Library from 01 January 2015 to 12 May 2025

ema.europa.eu Guiding Principles of Good AI Practice in Drug Development. fda.gov More resources Blogs GxP audit and inspection readiness what QA teams need to know Read more Webinars The evolution of quality intelligence activation Read more Webinars Activating regulatory intelligence with AI Read more

Practical considerations involve appropriate dosages, possible side effects, and consistent oversight from a medical provider