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Regulatory Affairs for
Biomaterials and Medical Devices
Edited by Amato & Ezzell, Published on October 2014, Pages: 202
Description :
All biomaterials and medical
devices are subject to a long list of regulatory practises and policies
which must be adhered to in order to receive clearance. This book provides
readers with information on the systems in place in the USA and the rest of
the world. Chapters focus on a series of procedures and policies including
topics such as commercialization, clinical development, general good
practise manufacturing and post market surveillance. |
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Polymeric Biomaterials: 2
Volume Set
Edited by Severian
Dumitriu & Valentin Popa, Published in 2013, Pages: 1710, Edition: 3rd
Description:
The book presents new
application chapters including Modular Biomimetic Drug Delivery Systems,
Biomedical Applications of Shape Memory Polymers and Their Nanocomposites,
Polymeric Gene Delivery Carriers for Pulmonary Diseases, and Bioceramics for
Development of Bioartificial Liver.
The book is organized into
two volumes containing 53 authoritative chapters written by experts from
around the world. The first volume, Polymeric Biomaterials: Structure and
Function, contains information about the structure and properties of
synthetic polymers including polyesters, polyphosphazenes, and elastomers
and natural polymers such as mucoadhesives, chitin, lignin, and carbohydrate
derivatives. It also describes their blends or composites-for example,
metal–polymer composites and biodegradable polymeric/ceramic composites-as
well as drug carriers and delivery systems, gene and nucleic acids delivery,
and polymer synthesis and processing techniques. |