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
TABLE OF CONTENTS
part |2 pages
Section I: Law, Business, and Commercialization
part |2 pages
Section II: Regulatory Issues and Nanogovernance
part |2 pages
Section III: Health, Safety, Risk, and Biological Interactions
part |2 pages
Section IV: Future Implications, Ethics, Perspectives, and Editorials