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This unique handbook (60 chapters) examines the entire "product
life cycle," from the creation of nanomedical products to their
final market introduction. While focusing on critical issues
relevant to nanoproduct development and translational activities,
it tackles topics such as regulatory science, patent law, FDA law,
ethics, personalized medicine, risk analysis, toxicology,
nano-characterization and commercialization activities. A separate
section provides fascinating perspectives and editorials from
leading experts in this complex interdisciplinary field.
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