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.
- ISBN13 9789814669221
- Publish Date 2 May 2016 (first published 27 April 2016)
- Publish Status Active
- Publish Country SG
- Imprint Pan Stanford Publishing Pte Ltd
- Format Hardcover
- Pages 1502
- Language English