Vol. XVIII · Free shipping $75+ · Read the collection
Feature · Product Review
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Description

Instead of classifying nanomedicines as a distinct category, regulatory bodies such as the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) emphasize a risk-based product-specific evaluation framework that calls for thorough physicochemical characterization, manufacturing reproducibility, biodistribution profiling, and safety assessment for drug products that contain nanomaterials

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Chng li cc tc nhn oxy ha, gc t do gip thi tr ton b ra khi c th

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Dis Sci (1996) 41:178693

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10.3390/ijms21145049 3 AgibalovaT.HempelA.MaurerH

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