8. Preclinical Development of a Pharmaceutical Product for Children

  1. Alan M. Hoberman4 and
  2. Elise M. Lewis5
  1. Graham P. Bailey1,
  2. Timothy P. Coogan2 and
  3. Luc M. De Schaepdrijver3

Published Online: 11 JAN 2012

DOI: 10.1002/9781118168226.ch8

Pediatric Nonclinical Drug Testing: Principles, Requirements, and Practices

Pediatric Nonclinical Drug Testing: Principles, Requirements, and Practices

How to Cite

Bailey, G. P., Coogan, T. P. and De Schaepdrijver, L. M. (2012) Preclinical Development of a Pharmaceutical Product for Children, in Pediatric Nonclinical Drug Testing: Principles, Requirements, and Practices (eds A. M. Hoberman and E. M. Lewis), John Wiley & Sons, Inc., Hoboken, NJ, USA. doi: 10.1002/9781118168226.ch8

Editor Information

  1. 4

    Research Department, Charles River Laboratories Preclinical Services, Horsham, PA, USA

  2. 5

    Elise M. Lewis, Reproductive and Neurobehavioral Toxicology, Charles River Preclinical Services, Horsham, PA, USA

Author Information

  1. 1

    Toxicology/Pathology - Global Preclinical Development J&J Pharmaceutical Research and Development, Division of Janssen, Beerse, Belgium

  2. 2

    Biologics Toxicology, Centocor Research & Development, Inc, Radnor, PA, USA

  3. 3

    Toxicology/Pathology Global Preclinical Development, Janssen R&D, a division of Janssen Pharmaceutica NV, Beerse, Belgium

Publication History

  1. Published Online: 11 JAN 2012
  2. Published Print: 27 JAN 2012

ISBN Information

Print ISBN: 9780470448618

Online ISBN: 9781118168226

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