design and conduct of clinical research. Writing Clinical Research Protocols includes practical information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents, getting protocols approved, special populations, confidentiality issues, and the reporting of adverse events. A valuable appendix includes a listing of web resources about research ethics as well as a glossary. This is an invaluable resource for basic scientists collaborating in clinical trials, physician investigators, clinical research fellows, research nurse coordinators, residents, and anyone who wants a better understanding of the clinical trials process.Walks investigators and trainees through identification of the ethical aspects of each section of a clinical research protocolIncludes a chapter containing Case HistoriesContains information on conducting clinical research within the pharmaceutical industryAn appendix includes internet resources and world wide web addresses for important research ethics documents and regulationsChapter on 'Study Design and Methodology' purposely expanded to explicitly address biostatistical considerations

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