CE Marking – (Conformité Européenne) It is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the
Food and Drug Administration (FDA) The US Food and Drug Administration (FDA) regulates AI-based Software as a Medical Device (SaMD) under the Federal Food, Drug, and Cosmetic Act
Regulatory bodies oversee the approval and usage of artificial intelligence (AI) technologies in radiology to ensure their safety, efficacy, and quality. Different countries and regions
