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 medicin
Section I - Law, Business and Commercialization. Section II - Regulatory Issues and Nanogovernance. Section III - Health, Safety, Risk and Biological Interactions. Section IV - Future Implications, Ethics and Perspectives.
