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Handbook of Clinical Nanomedicine : Law, Business, Regulation, Safety and Risk

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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 Read more...

Abstract: 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

Author(s): Bawa, Raj
Series: Pan Stanford series on nanomedicine 1
Publisher: [s.n.]
Year: 2015

City: S.l
Tags: Специальные дисциплины;Наноматериалы и нанотехнологии;Нанобиотехнология;

Content: Section 1. General introduction and beginnings --
section 2. Nanoparticles, nanodevices, and imaging --
section 3. Therapy and clinical applications.