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Writing Clinical Research Protocols

Ethical Considerations

1st Edition - August 4, 2005

Authors: Evan DeRenzo, Joel Moss

Language: English
Paperback ISBN:
9 7 8 - 0 - 1 2 - 2 1 0 7 5 1 - 1
eBook ISBN:
9 7 8 - 0 - 0 8 - 0 4 5 4 2 0 - 7

This highly engaging guide for clinical researchers provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical… Read more

Writing Clinical Research Protocols

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This highly engaging guide for clinical researchers provides a foundation for improving skills in the understanding of ethical requirements in the 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.