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Drugs between Research and Regulations

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Cover of 'Drugs between Research and Regulations'

Table of Contents

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    Book Overview
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    Chapter 1 Chronic toxicity tests, current problems and possible solutions
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    Chapter 2 What can be gained from a retrospective analysis of chronic toxicity studies?
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    Chapter 3 The role of carcinogenicity studies in risk assessment
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    Chapter 4 Alternatives to chronic toxicity studies
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    Chapter 5 What good are clinical trials?
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    Chapter 6 Clinical guidelines — a help or a hindrance?
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    Chapter 7 Clinical trials in the natural environment
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    Chapter 8 Clinical trials and the general practitioner
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    Chapter 9 Clinical trials and chronic diseases
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    Chapter 10 Alternatives to clinical trials in post-marketing research on drug effects
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    Chapter 11 The future of long-term intervention and prevention studies — methodological aspects
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    Chapter 12 Lessons for the future from long-term studies with beta blockers and hypolipidaemic agents
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    Chapter 13 Rauwolfia derivatives and breast cancer: how do we know when we have the answers?
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    Chapter 14 The organisation of long-term intervention and prevention studies
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    Chapter 15 The explanatory and pragmatic approaches in clinical trials
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    Chapter 16 Alternatives to classical randomized trials
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    Chapter 17 Data quality assurance with particular regard to protocol violations
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    Chapter 18 The need of clinical drug trials in children
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    Chapter 19 Ethical restrictions in clinical trials in children
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    Chapter 20 The role of the EEC in the harmonisation of drug registration
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    Chapter 21 Clinical trials — European recommendations
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    Chapter 22 The Pharmaceutical Industry — research and responsibility
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Title
Drugs between Research and Regulations
Published by
Steinkopff, April 2013
DOI 10.1007/978-3-642-54130-8
ISBNs
978-3-64-254132-2, 978-3-64-254130-8
Editors

Steichele, C., Abshagen, U., Koch-Weser, J.

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