Description

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.

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

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£420.00

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Hardback by Raj Bawa , Gerald F. Audette

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Short Description:

This unique handbook (60 chapters) examines the entire "product life cycle," from the creation of nanomedical products to their final... Read more

    Publisher: Pan Stanford Publishing Pte Ltd
    Publication Date: 02/05/2016
    ISBN13: 9789814669221, 978-9814669221
    ISBN10: 9814669229

    Number of Pages: 1502

    Non Fiction , Education

    Description

    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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