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- W2950576572 endingPage "43" @default.
- W2950576572 startingPage "23" @default.
- W2950576572 abstract "After decades of research, nanotechnology has been used in a broad array of biomedical products including medical devices, drug products, drug substances, and pharmaceutical-grade excipients. But like many great achievements in science, there is a fine balance between the risks and opportunities of this new technology. Some materials and surface structures in the nanosize range can exert unexpected toxicities and merit a more detailed safety assessment. Regulatory agencies such as the United States Food and Drug Administration or the European Medicines Agency have started dealing with the potential risks posed by nanomaterials. Considering that a thorough characterization is one of the key aspects of controlling such risks this review presents the regulatory background of nanosafety assessment and provides some practical advice on how to characterize nanomaterials and drug formulations. Further, the challenges of how to maintain and monitor pharmaceutical quality through a highly complex production processes will be discussed." @default.
- W2950576572 created "2019-06-27" @default.
- W2950576572 creator A5003617237 @default.
- W2950576572 creator A5009072438 @default.
- W2950576572 creator A5023454374 @default.
- W2950576572 creator A5054757705 @default.
- W2950576572 creator A5057276398 @default.
- W2950576572 creator A5083340646 @default.
- W2950576572 date "2019-11-01" @default.
- W2950576572 modified "2023-10-02" @default.
- W2950576572 title "Nanomedicines - Tiny particles and big challenges" @default.
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