The enormous advances in nanomedicine in the past decade have
necessitated a growing need for an authoritative and comprehensive
reference source that can be relied upon by scientists, clinicians,
students, and industry and policy makers alike. The Handbook of
Clinical Nanomedicine: From Bench to Bedside is designed to offer a
global perspective on the wonders of nanomedicine.
The handbook aims to provide a broad survey of various
interconnected topics pertaining to nanomedicine. It is intended to
be a stand-alone, easily accessible volume that examines the entire
"product wheel" from creation of nanomedical products to final
market introduction, all accomplished in a user-friendly format.
Specifically, everything from bio-nanomaterials and nanodevices
from the R&D stage to patent protection, clinical regulatory
aspects, and eventual commercialization is encompassed in this
book. In addition to highlighting cutting-edge technologies, the
book addresses critical topics such as ethics, safety and toxicity,
environmental health, nanoeconomics, business strategy, licensing,
intellectual property, FDA law, EPA law, and governmental policy
issues. With contributions from international experts, the diverse
team of editors has compiled a book that provides a unified
perspective to these varied topics. While many books focus on
nanomedicine, nanotechnology, or nanoscience, none provide the
medical applications of nanotechnology with both a clinical and
business angle. Furthermore, most of the currently available books
on the market fail to highlight the truly global nature of
nanomedicine.
The handbook, divided into four sections, provides a
comprehensive road map of basic research in nanomedicine as well as
clinical applications and commercialization activities. Each of the
45-plus chapters contains 10 20 key words, extensive tables, color
figures, future projections, and an extensive list of references.
The handbook is an essential reading for the novice and expert
alike in fields such as medicine, law, biotechnology,
pharmaceutical sciences, engineering, biomedicine, policy, future
studies, ethics, intellectual property law, licensing, and
toxicology. While bridging the gap between basic biomedical
research, engineering, and medicine, the handbook provides an
understanding of nanotechnology s
- use to solve medical problems
- current applications and their potential
- regulatory environment and policy issues
- intellectual property, licensing, and business activities
It is clear that the well-known editors have skillfully selected
and thoroughly edited each chapter to reflect the most updated
information possible. The range of topics covered as well as the
international selection of authors is truly impressive. Since the
rapidly evolving field of nanomedicine is very diverse and covers
physical, chemical, biological, and engineering aspects, the range
of the contributing authors accurately reflects this. The book s
multidisciplinary approach and an in-depth focus on nanomedicine,
pharmaceutical sciences, materials science, biomedical engineering,
and biotechnology will attract a global audience. In short,
Handbook of Clinical Nanomedicine: From Bench to Bedside promises
to be a standard reference text in this expansive and
interdisciplinary field. It is a timely addition to the literature
on nanosciences and will undoubtedly serve as a catalyst to
stimulate interest in this rapidly growing field."
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