Biocompatibility and Performance of Medical Devices
- 2nd Edition - November 20, 2019
- Latest edition
- Editor: Jean-Pierre Boutrand
- Language: English
Biocompatibility and Performance of Medical Devices, Second Edition, provides an understanding of the biocompatibility and performance tests for ensuring that biomateri… Read more
Description
Description
Biocompatibility and Performance of Medical Devices, Second Edition, provides an understanding of the biocompatibility and performance tests for ensuring that biomaterials and medical devices are safe and will perform as expected in the biological environment. Sections cover key concepts and challenges faced in relation to biocompatibility in medical devices, discuss the evaluation and characterization of biocompatibility in medical devices, describe preclinical performance studies for bone, dental and soft tissue implants, and provide information on the regulation of medical devices in the European Union, Japan and China. The book concludes with a review of histopathology principles for biocompatibility and performance studies.
Key features
Key features
- Presents diverse insights from experts in government, industry and academia
- Delivers a comprehensive overview of testing and interpreting medical device performance
- Expanded to include new information, including sections on managing extractables, accelerating and simplifying medical device development through screening and alternative biocompatibility methods, and quality strategies which fasten device access to market
Readership
Readership
Scientists and researchers in medical device technology or government agencies:
Biocompatibility scientists, regulatory affairs professionals, product development engineers, preclinical scientists, applied researchers
Table of contents
Table of contents
Part One Introduction to biocompatibility in medical devices 000
1 Strategies to accelerate medical market access and manage risks of biocompatibility
R. Eloy and S.J. Goldenberg
2 Making use of a biological safety evaluation plan
D. Parente
3 Biomechanical and biochemical compatibility in innovative biomaterials
J. Huang, X. Li, and Z.X. Guo
Part Two Evaluation and characterization of biocompatibility in medical devices
4 A practical approach to analytical chemistry of medical devices
D.E. Albert
5 Tolerable intake values for leachables: Practical use of ISO 10993-17 standard
R.P. Brown
6 In vivo and in vitro testing for the biological safety evaluation of biomaterials and medical devices
W.H. De Jong, J.W. Carraway, and R.E. Geertsma
7 Practical approach to blood compatibility assessments: General considerations and standards
M.F. Wolf and J.M. Anderson
8 Quality strategies that fasten devices access to global markets
J.A. Torfin and S. Gompertz
9 Accelerating medical device biocompatibility evaluation: An industry perspective
K.P. Coleman, W.V. Christian, and W. Zhang
10 Overcoming negative test results during manufacture
D. Parente
11 Methods for the characterization and evaluation of drug-device combination products
A.L. Lewis
Part Three Testing and interpreting the performance of medical devices
12 Efficient evaluations of bone implants performances
J.-P. Boutrand
13 Methods and interpretation of performance studies for dental implants
M. Dard
14 Optimizing the design of preclinical safety and performance studies—Examples in soft tissues and cardio-vascular implants
E. Drevon-Gaillot, T. Blair, and G. Clermont
15 Mechanical testing for soft and hard tissue implants
C. Kaddick
Part Four International regulation of medical devices
16 Biological evaluation and regulation of medical devices in the European Union
T. Keene
17 Biological evaluation and regulation of medical devices in Japan
K. Kojima and K. Sakaguchi
18 Medical device regulations in China
C. Shan and M. Liu
Part Five Histopathology principles for biocompatibility and performance studies
19 Current considerations in medical device pathology
A. Alves, L. Wancket, A. Metz
Product details
Product details
- Edition: 2
- Latest edition
- Published: November 21, 2019
- Language: English
About the editor
About the editor
JB
Jean-Pierre Boutrand
Jean-Pierre (JP) Boutrand, DVM, MS is a Senior Vice President at Eurofins, Luxembourg.
Dr. Boutrand is an executive leader, veterinarian, and recognized authority in nonclinical evaluation, biological safety, and testing strategies for medical devices and combination products. With over 25 years of global leadership—including senior executive roles at NAMSA (Vice President of Global Laboratory Services), Labcorp, Charles River Laboratories and Eurofins—Dr. Boutrand has guided the safety, compliance, and commercialization pathways for hundreds of complex medical devices worldwide. A former registered expert on the biological safety of medical devices for regulatory agencies including ANSM, Dr. Boutrand specialized in integrated risk management, ISO 10993 compliance, toxicology assessment strategies, and pharmacology models. He is the editor and author of the textbook Biocompatibility and Performance of Medical Devices (Woodhead Publishing / Elsevier), currently in its 3rd edition, and has authored over 120 scientific publications and global conference presentations on biomaterial safety, histopathology, and regulatory evaluation frameworks.