Section 1. General introduction and beginnings --; section 2. Nanoparticles, nanodevices, and imaging --; section 3. Therapy and clinical applications.
SUMMARY OR ABSTRACT
Text of Note
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.