Biocompatibility and Performance of Medical Devices (Woodhead Publishing Series in Biomaterials)

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9780857090706: Biocompatibility and Performance of Medical Devices (Woodhead Publishing Series in Biomaterials)

Implant and device manufacturers are increasingly facing the challenge of proving that their products are safe and biocompatible, and that they will perform as expected. Biocompatibility and performance of medical devices provides an essential guide to the performance analysis of these vital devices.

Part one introduces the key concepts and challenges faced in relation to biocompatibility in medical devices, with consideration of biological safety evaluation planning and biomechanical and biochemical compatibility in innovative biomaterials. Part two goes on to discuss the evaluation and characterisation of biocompatibility in medical devices. Topics covered include material and chemical characterisation, allowable limits for toxic leachables, in vivo and in vitro testing and blood compatibility assessment. Testing and interpreting medical device performance is the focus of part three, with chapters describing preclinical performance studies for bone, dental and soft tissue implants, and mechanical testing of soft and hard tissue implants. Part four provides information on the regulation of medical devices in the European Union, Japan and China, and the book concludes with part five, a review of histopathology principles for biocompatibility and performance studies.

With its distinguished editor and international team of expert contributors, Biocompatibility and performance of medical devices is a vital tool for all those involved in the research, design, production and application of medical devices, including research directors, production companies and medical regulatory agencies, as well as industry professionals and academics.

  • Examines the key concepts and challenges faced in relation to biocompatibility in medical devices
  • Discusses evaluation and characterisation issues, including material and chemical characterization, allowable limits for toxic leachables, in vivo and in vitro testing, and blood compatibility assessment
  • Delivers a comprehensive overview of testing and interpreting medical device performance

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About the Author:

Jean-Pierre Boutrand is General Manager and Scientific Director for the European division of NAMSA (the world leading medical device evaluation company). Dr Boutrand has been involved in more than 100 public presentations and publications on topics related to medical device evaluation and is registered as an expert on the biological safety of medical devices for ANSM (the French agency for the safety of health products).

Review:

Multiple authors ... have come together to present their views on the best options, the best techniques and the optimal methods of interpretation of data. Expertly assembled by Jean-Pierre Boutrand ... the contents of this book will allow the reader to attain an insight into the complexities of this testing arena., Professor David Williams, Wake Forest Baptist Medical Center, USA (from the Foreword)

"About this title" may belong to another edition of this title.

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Published by Woodhead Publishing (2017)
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Book Description ELSEVIER SCIENCE TECHNOLOGY, United Kingdom, 2012. Hardback. Book Condition: New. Language: English . This book usually ship within 10-15 business days and we will endeavor to dispatch orders quicker than this where possible. Brand New Book. Implant and device manufacturers are increasingly facing the challenge of proving that their products are safe and biocompatible, and that they will perform as expected. Biocompatibility and performance of medical devices provides an essential guide to the performance analysis of these vital devices.Part one introduces the key concepts and challenges faced in relation to biocompatibility in medical devices, with consideration of biological safety evaluation planning and biomechanical and biochemical compatibility in innovative biomaterials. Part two goes on to discuss the evaluation and characterisation of biocompatibility in medical devices. Topics covered include material and chemical characterisation, allowable limits for toxic leachables, in vivo and in vitro testing and blood compatibility assessment. Testing and interpreting medical device performance is the focus of part three, with chapters describing preclinical performance studies for bone, dental and soft tissue implants, and mechanical testing of soft and hard tissue implants. Part four provides information on the regulation of medical devices in the European Union, Japan and China, and the book concludes with part five, a review of histopathology principles for biocompatibility and performance studies.With its distinguished editor and international team of expert contributors, Biocompatibility and performance of medical devices is a vital tool for all those involved in the research, design, production and application of medical devices, including research directors, production companies and medical regulatory agencies, as well as industry professionals and academics. Bookseller Inventory # EOD9780857090706

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Published by ELSEVIER SCIENCE TECHNOLOGY, United Kingdom (2012)
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Book Description ELSEVIER SCIENCE TECHNOLOGY, United Kingdom, 2012. Hardback. Book Condition: New. Language: English . Brand New Book. Implant and device manufacturers are increasingly facing the challenge of proving that their products are safe and biocompatible, and that they will perform as expected. Biocompatibility and performance of medical devices provides an essential guide to the performance analysis of these vital devices.Part one introduces the key concepts and challenges faced in relation to biocompatibility in medical devices, with consideration of biological safety evaluation planning and biomechanical and biochemical compatibility in innovative biomaterials. Part two goes on to discuss the evaluation and characterisation of biocompatibility in medical devices. Topics covered include material and chemical characterisation, allowable limits for toxic leachables, in vivo and in vitro testing and blood compatibility assessment. Testing and interpreting medical device performance is the focus of part three, with chapters describing preclinical performance studies for bone, dental and soft tissue implants, and mechanical testing of soft and hard tissue implants. Part four provides information on the regulation of medical devices in the European Union, Japan and China, and the book concludes with part five, a review of histopathology principles for biocompatibility and performance studies.With its distinguished editor and international team of expert contributors, Biocompatibility and performance of medical devices is a vital tool for all those involved in the research, design, production and application of medical devices, including research directors, production companies and medical regulatory agencies, as well as industry professionals and academics. Bookseller Inventory # AAZ9780857090706

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Published by ELSEVIER SCIENCE TECHNOLOGY, United Kingdom (2012)
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Book Description ELSEVIER SCIENCE TECHNOLOGY, United Kingdom, 2012. Hardback. Book Condition: New. New.. Language: English . Brand New Book. Implant and device manufacturers are increasingly facing the challenge of proving that their products are safe and biocompatible, and that they will perform as expected. Biocompatibility and performance of medical devices provides an essential guide to the performance analysis of these vital devices.Part one introduces the key concepts and challenges faced in relation to biocompatibility in medical devices, with consideration of biological safety evaluation planning and biomechanical and biochemical compatibility in innovative biomaterials. Part two goes on to discuss the evaluation and characterisation of biocompatibility in medical devices. Topics covered include material and chemical characterisation, allowable limits for toxic leachables, in vivo and in vitro testing and blood compatibility assessment. Testing and interpreting medical device performance is the focus of part three, with chapters describing preclinical performance studies for bone, dental and soft tissue implants, and mechanical testing of soft and hard tissue implants. Part four provides information on the regulation of medical devices in the European Union, Japan and China, and the book concludes with part five, a review of histopathology principles for biocompatibility and performance studies.With its distinguished editor and international team of expert contributors, Biocompatibility and performance of medical devices is a vital tool for all those involved in the research, design, production and application of medical devices, including research directors, production companies and medical regulatory agencies, as well as industry professionals and academics. Bookseller Inventory # AAZ9780857090706

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Book Description Woodhead Publishing, 2012. Book Condition: New. This book describes and explains the factors that influence the biocompatibility of materials and medical devices. Editor(s): Boutrand, Jean-Pierre. Series: Woodhead Publishing Series in Biomaterials. Num Pages: 544 pages, Illustrations. BIC Classification: MQW. Category: (UP) Postgraduate, Research & Scholarly. Dimension: 243 x 163 x 36. Weight in Grams: 998. . 2012. 1st Edition. Hardcover. . . . . . Bookseller Inventory # V9780857090706

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Book Description Woodhead Publishing. Book Condition: New. This book describes and explains the factors that influence the biocompatibility of materials and medical devices. Editor(s): Boutrand, Jean-Pierre. Series: Woodhead Publishing Series in Biomaterials. Num Pages: 544 pages, Illustrations. BIC Classification: MQW. Category: (UP) Postgraduate, Research & Scholarly. Dimension: 243 x 163 x 36. Weight in Grams: 998. . 2012. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland. Bookseller Inventory # V9780857090706

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