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FDA Encourages Innovation and Safety as Part of Medical Device Regulatory Overhaul EAS authored an article in MedTech Intelligence on FDAs efforts at encouraging innovation while keeping a close eye on safety as part of a medical device regulatory overhaul

70 countries classify and regulate e-cigarettes uniquely as vaping products, 57 as tobacco products on the same level as classic combustible cigarettes, 18 as consumer products/devices, and 4 as poisons or hazardous substances due to their lack of medicinal purpose [73]

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