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Produktbild: The Textbook of Pharmaceutical Medicine

The Textbook of Pharmaceutical Medicine

375,99 €

inkl. gesetzl. MwSt., Versandkostenfrei


Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

10.05.2013

Herausgeber

John P. Griffin + weitere

Verlag

John Wiley & Sons

Seitenzahl

856

Maße (L/B/H)

25,1/17,7/4,5 cm

Gewicht

1416 g

Auflage

7th edition

Sprache

Englisch

ISBN

978-0-470-65987-8

Beschreibung

Rezension

"This comprehensive volume covers the processes by which medicines are developed, tested and approved. The chapters are written by leading academics, medical directors and legal experts in the field of harmaceutical medicine and provide authorative and in-depth information for both physicians working in and those who are currently training in the pharmaceutical industry." (British Journal of Clinical Pharmacology, 22 April 2014)
 
"This book is expected to be useful for pharmaceutical physicians and for anyone interested in learning about the various issues in drug discovery and development. In addition to many other topics, the regulatory aspects of drug development in the U.S., Europe, and Japan are well covered . . . Nevertheless, this is an admirable effort and the book deserves a place on the bookshelves of pharmaceutical physicians. " (Doody's, 30 August 2013)

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

10.05.2013

Herausgeber

Verlag

John Wiley & Sons

Seitenzahl

856

Maße (L/B/H)

25,1/17,7/4,5 cm

Gewicht

1416 g

Auflage

7th edition

Sprache

Englisch

ISBN

978-0-470-65987-8

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

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  • Produktbild: The Textbook of Pharmaceutical Medicine
  • Contributors
     
    The editors
     
    Acknowledgements
     
    List of abbreviations
     
    Preface
     
    Part I Research and development
     
    1 Discovery of new medicines
    Yves J. Ribeill
     
    2 Pharmaceutical development
    Michael Gamlen and Paul Cummings
     
    3 Preclinical safety testing
    Lutz Müller and Elisabeth Husar
     
    4 Exploratory development
    John Posner
     
    5 Clinical pharmacokinetics
    Paul Rolan and Valéria Molnár
     
    6 Biological therapeutics
    Peter Lloyd and Jennifer Sims
     
    7 Objectives and design of clinical trials
    John Posner and Steve Warrington
     
    8 Conduct of clinical trials: Good Clinical Practice
    Kate L.R. Darwin
     
    9 Medical statistics
    Andrew P. Grieve
     
    10 Development of medicines: full development
    Peter D. Stonier
     
    11 Pharmacovigilance
    Stephen F. Hobbiger, Bina Patel and Elizabeth Swain
     
    12 Vaccines
    John Beadle
     
    13 Drugs for cancer
    James Spicer and Johann De Bono
     
    14 Ethics of human experimentation
    Jane Barrett
     
    15 Drug development in paediatrics and neonatology
    Nazakat M. Merchant and Denis V. Azzopardi
     
    16 Due diligence and the role of the pharmaceutical physician
    Geoffrey R. Barker
     
    Part II Regulation
     
    17 A history of drug regulation in the UK
    John P. Griffin
     
    18 The Clinical Trials Directive
    Fergus Sweeney and Agnès Saint Raymond
     
    19 Human medicinal products in the European Union: Regulations, Directives and structures
    Agnès Saint Raymond and Anthony J. Humphreys
     
    20 Human medicinal products in the European Union: Procedures
    Agnès Saint Raymond and Anthony J. Humphreys
     
    21 European regulation of medical devices
    Shuna Mason
     
    22 Paediatric regulation
    Heike Rabe and Agnès Saint-Raymond
     
    23 Technical requirements for registration of pharmaceuticals for human use: The ICH process
    Dean W.G. Harron
     
    24 The regulation of drug products by the US Food and Drug Administration
    Peter Barton Hutt
     
    25 The US FDA in the drug development, evaluation and approval process
    Richard N. Spivey, Judith K. Jones, William Wardell and William W. Vodra
     
    26 Future prospects of the pharmaceutical industry and its regulation in the USA
    Richard N. Spivey, William W. Vodra, Judith K. Jones and William Wardell
     
    27 Regulatory and clinical trial systems in Japan
    Mamiko Satake and Natsuko Hosoda
     
    28 The regulation of therapeutic products in Australia
    Elizabeth de Somer, Deborah Monk and Janice Hirshorn
     
    Part III Health care marketplace
     
    29 An Introduction to life cycle management of medicines
    David Gillen
     
    30 Availability of medicines online and counterfeit medicines
    Ruth Diazaraque and David Gillen
     
    31 The supply of unlicensed medicines for individual patient use
    Ian Dodds-Smith and Ewan Townsend
     
    32 Legal and ethical issues relating to medicinal products
    Nick Beckett, Sarah Hanson and Shuna Mason
     
    33 Medical marketing
    David B. Galloway and Bensita M.V. Thottakam
     
    34 Information and promotion
    Charles De Wet
     
    35 Economics of health care
    Carole A. Bradley and Jane R. Griffin
     
    36 Controls on NHS medicines prescribing and expenditure in the UK (a historical perspective) with some international comparisons
    John P. Griffin and Geoffrey R. Barker
     
    37 Pharmaceutical medicine in the emerging markets
    Nadarajah Sreeharan, Jennie A. Sykes and Richard B. Nieman
     
    38 Biosimilars
    Raymond A. Huml and John Posner
     
    Appendix 1 Declaration of Helsinki
     
    Appendix 2 Agreements and Guidelines for Implementation of Clinical Trials
     
    Appendix 3 D