International Labeling Requirements for Medical Devices, Medical Equipment and Diagnostic Products

Author:   Charles Sidebottom
Publisher:   Taylor & Francis Inc
Edition:   2nd edition
ISBN:  

9780849318504


Pages:   616
Publication Date:   27 June 2003
Format:   Hardback
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

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International Labeling Requirements for Medical Devices, Medical Equipment and Diagnostic Products


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Overview

"Extensively revised, with an updated title that reflects its expanded scope, International Labeling Requirements for Medical Devices, Medical Equipment, and Diagnostic Products, Second Edition provides the practical labeling information you need to achieve rapid regulatory approval, gain marketplace acceptance, and assure user comprehension. A complete guide to all aspects of advertising, labeling, and packaging, the book explains the relevant laws, regulations, and requirements in major markets worldwide. Coverage includes requirements such as text, dimensions, type sizes, graphic elements, symbols, and language for implantable devices, sterile devices, OTC products, in vitro diagnostic products, radiation emitting devices, contraceptive devices, and more. This is not a ""cookbook"" of easy-to-follow recipes. It is a comprehensive resource that gives you the tools to stay ahead in the ever-changing regulatory environment."

Full Product Details

Author:   Charles Sidebottom
Publisher:   Taylor & Francis Inc
Imprint:   CRC Press Inc
Edition:   2nd edition
Dimensions:   Width: 21.00cm , Height: 8.60cm , Length: 28.00cm
Weight:   2.630kg
ISBN:  

9780849318504


ISBN 10:   0849318505
Pages:   616
Publication Date:   27 June 2003
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

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an asset to the medical device industrycontinues to provide practical guidance for industry to facilitate international regulatory approvals and appropriately educate users in today's environment. - From the foreword by Charles H. Swanson, Ph.D., Vice President and Chief Regulatory Officer, Medtronic, Inc. Promo Copy


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Sidebottom, Charles

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