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Established in 1997, the Food and Drugs Authority (FDA) draws its mandate from Part 6, 7 and 8 of the Public Health Act, 2012 (Act 851), to provide and enforce standards for the manufacture, import, export, sale and distribution of food, drugs (herbal/allopathic/veterinary), cosmetics, medical devices, household chemical substances, tobacco and tobacco products, blood and blood products and the regulation of Clinical Trials in a bid to safeguard public health and safety

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Do Child Medical Consent Laws Vary by State