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Table of contents

  1. Front Matter
    Pages i-xiii
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  2. Introduction
    R. B. Smith
    Pages 1-7
  3. Discovery
    R. B. Smith
    Pages 9-19
  4. Basic Scientific Characterisation
    R. B. Smith
    Pages 21-44
  5. Safety Evaluation (Animal Studies)
    R. B. Smith
    Pages 45-51
  6. Formulation Development
    R. B. Smith
    Pages 53-62
  7. Human Pharmacology
    R. B. Smith
    Pages 63-70
  8. Evaluation of Human Efficacy and Safety
    R. B. Smith
    Pages 71-88
  9. The Regulatory Process
    R. B. Smith
    Pages 89-97
  10. Marketing
    R. B. Smith
    Pages 99-105
  11. Project Co-ordination
    R. B. Smith
    Pages 107-109
  12. Manufacture and Supply
    R. B. Smith
    Pages 111-116
  13. The Post-registration Phase
    R. B. Smith
    Pages 117-126
  14. International Development
    R. B. Smith
    Pages 127-133
  15. Risk —Benefit Ratio
    R. B. Smith
    Pages 135-141
  16. Integration and Innovation
    R. B. Smith
    Pages 143-145
  17. The Organisation
    R. B. Smith
    Pages 147-152
  18. The Future
    R. B. Smith
    Pages 153-158
  19. Back Matter
    Pages 159-159
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About this book

Keywords

development history medicine

Authors and affiliations

  • R. B. Smith
    • 1
  1. 1.St Bartholomew’s HospitalLondonUK

Bibliographic information

  • DOI https://doi.org/10.1007/978-1-349-17954-1
  • Copyright Information Macmillan Publishers Limited 1985
  • Publisher Name Palgrave, London
  • eBook Packages Engineering
  • Print ISBN 978-0-333-36885-5
  • Online ISBN 978-1-349-17954-1
  • Buy this book on publisher's site