Regulatory Affairs for Biomaterials and Medical Devices, 1st Edition, Publication Date: December 2014, Author(s): Steve Amato (Editor), R Ezzell (Editor), Publisher: Woodhead Publishing, ISBN: 9780857095428, Print Book: Hardcover

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Regulatory Affairs for Biomaterials and Medical Devices, 1st Edition, Publication Date: December 2014, Author(s): Steve Amato (Editor), R Ezzell (Editor), Publisher: Woodhead Publishing, ISBN: 9780857095428, Print Book: Hardcover

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Products Details

 

Series: Woodhead Publishing Series in Biomaterials (Book 79)

Hardcover: 202 pages

Publisher: Woodhead Publishing; 1 edition (December, 2014)

Language: English

ISBN-10: 0857095420

ISBN-13: 978-0857095428

Product Dimensions: 0.8 x 6 x 9 inches

Shipping Weight: 1 pounds

 

Key Features

 

  • Addresses global regulations and regulatory issues surrounding biomaterials and medical devices
  • Especially useful for smaller companies who may not employ a full time vigilance professional
  • Focuses on procedures and policies including risk management, intellectual protection, marketing authorisation, university patent licenses and general good practise manufacturing

 

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.

Readership

Regulatory managers within industry and academia; Entrepreneurs in the field

 

Table of Contents

 

1 Biomaterials and their applications in medicine
I. Kulinets, Northeastern University, USA

2 Technical considerations for the commercialization of biomaterials
N. Scarborough, NLS Consulting, USA and N. Mukherjee, Covidien, USA

3 Regulatory strategies for biomaterials and medical devices in the USA: Classification, design and risk analysis
S. F. Amato, Northeastern University, USA

4 Clinical development and endpoint strategies for biomaterials and medical devices
S. F. Amato, Northeastern University, USA

5 The clinical evaluation and approval threshold of biomaterials and medical devices
K. G. Stevens, DePuy Synthes Spine, USA

6 Supply chain controls for biomaterials and medical devices in the USA
S. F. Amato, Northeastern University, USA

7 Global marketing authorisation of biomaterials and medical devices
J. J. Tobin, ChemHaz Solutions, Ireland

8 Good manufacturing practice (GMP) for biomaterials and medical devices in the EU and the USA
F. Tarabah, Strategiqual, France

9 Post market surveillance approaches for biomaterials and medical devices in the USA
K. Desai, Northeastern University, USA

10 Fundamentals of medical device approval in Asia
J. L. Wong, ARPA, Hong Kong and P. Teysseyre, Johnson & Johnson Medical Asia Pacific, Singapore

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