Chapter 9. Medical Devices

  1. Dr. John J. Tobin1 and
  2. Prof. Dr. Gary Walsh2

Published Online: 12 SEP 2008

DOI: 10.1002/9783527623037.ch9

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

How to Cite

Tobin, J. J. and Walsh, G. (2008) Medical Devices, in Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany. doi: 10.1002/9783527623037.ch9

Author Information

  1. 1

    ChemHaz Solutions Ltd., Laccaroe, Feakle, County Clare, Ireland

  2. 2

    Chemical and Environmental Sciences Department, University of Limerick, Castletroy, Limerick City, Ireland

Publication History

  1. Published Online: 12 SEP 2008
  2. Published Print: 9 JUL 2008

ISBN Information

Print ISBN: 9783527318773

Online ISBN: 9783527623037

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Keywords:

  • device classification;
  • development;
  • design controls

Summary

This chapter contains sections titled:

  • Chapter Introduction

  • Regulatory Strategy for Medical Devices in the EU

  • Regulatory Strategy for Medical Devices in the US

  • Development of Devices

  • Chapter Review

  • Further Reading