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Item Details
Title: WRITING CLINICAL RESEARCH PROTOCOLS
ETHICAL CONSIDERATIONS
By: Evan DeRenzo (Editor), Joel Moss (Editor)
Format: Paperback

List price: £52.99


We currently do not stock this item, please contact the publisher directly for further information.

ISBN 10: 0122107519
ISBN 13: 9780122107511
Publisher: ELSEVIER SCIENCE PUBLISHING CO INC
Pub. date: 15 January, 2005
Pages: 320
Description: Intended for clinical researchers, this book provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents.
Synopsis: 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.
Publication: US
Imprint: Academic Press Inc
Returns: Non-returnable
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