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- 128 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
eBook - ePub
Book details
Table of contents
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About This Book
This volume provides an introduction to the process of clinical drug development. It demystifies the way new medicines are discovered, tested and regulated. This book is intended for those who wich to understand the background of clinical trials from a pharmaceutical company perspective, and is suitable for clinical trials supplies technicians and pharmacists, data management staff, information officers, medical secretaries and all support staff. This second edition is updated and includes information on the practical implications of recent EC legislation.
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Yes, you can access Clinical Trials by Ann Raven, Frank Wells in PDF and/or ePUB format, as well as other popular books in Medicine & Public Health, Administration & Care. We have over one million books available in our catalogue for you to explore.
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Table of contents
- Cover
- Half Title
- Title Page
- Copyright Page
- Contents
- Foreword
- Preface
- Acknowlegements
- About the Author
- 1 Drug Development
- 2 Regulation of Drug Research
- 3 Good Clinical Practice
- 4 Clinical Investigators
- 5 Trial Design and Protocols
- 6 Case Record Forms
- 7 Trial Supplies
- 8 Clinical Research Associates
- 9 Monitoring and Adverse Events
- 10 Analysis and Reports
- 11 Standard Operating Procedures (SOPs), Audits and Archives
- Appendix 1: Glossary of Abbreviations
- Appendix 2: Glossary of Terms
- Appendix 3: Further Reading
- Appendix 4: Use of Medical Qualifications (UK)
- Appendix 5: Commonly Used Qualifications (UK)
- Appendix 6: Questions for Group Discussion
- Appendix 7: World Medical Association Declaration of Helsinki
- Appendix 8: EC Note for Guidance: Good clinical practice for trials on medicinal products in the European Community
- Index