A Comparative Study of Drug Regulatory Frameworks: United States FDA vs. European Medicines Agency
DOI:
https://doi.org/10.48047/Keywords:
.Abstract
This paper presents a comparative analysis of the United States Food and Drug Administration (USFDA) and the European Medicines Agency (EMA), focusing on their drug regulatory frameworks, approval pathways, safety monitoring, and post-marketing surveillance systems. The study identifies key similarities and differences in their approaches
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