Designing Clinical Research. This item is unavailable.
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Language: English
Published by LWW, 2013
- Softcover
- Used

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Softcover
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- Title
- Designing Clinical Research
- Author
- Newman MD MPH, Thomas B,Grady MD MPH, Deborah G,Browner MD MPH, Warren S,Cummings MD, Steven R,Hulley MD MPH, Dr. Stephen B
- Publisher
- LWW
- Publication year
- 2013
- Condition
- Good
- Binding
- Paperback
- Language
- English
- ISBN 10
- 1608318044
- ISBN 13
- 9781608318049
- Edition
- 4th Edition
Designing Clinical Research has been extensively revised and continues to set the standard as a practical guide for doctors, nurses, pharmacists, and other health professionals involved in all forms of clinical, translational, and public health research. It presents advanced epidemiologic concepts in a reader-friendly way, and suggests common sense approaches to the challenging judgments involved in designing, funding, and implementing. New to this edition: Expanded and updated content in every chapter, with new material on: non-inferiority trials for comparative effectiveness research; incidence-density case-control studies; confounding and effect modification; diagnostic test studies to inform prediction rules; ethical aspects of whole genome sequencing; automated data management approaches; new NIH grant-writing requirements n Color format, and Electronic access, powered by Inkling[trademark] as a free companion to the text; viewable through your browser or as a download to tablet or smartphone; the complete text with optimized navigation; note-sharing, highlighting and bookmarking capability; cross-linking of references and content; and, rapid search options linked to the new glossary.
"Synopsis" may belong to another edition of this title.
Product Description
Designing Clinical Research has been extensively revised and continues to set the standard as a practical guide for doctors, nurses, pharmacists, and other health professionals involved in all forms of clinical, translational, and public health research. It presents advanced epidemiologic concepts in a reader-friendly way, and suggests common sense approaches to the challenging judgments involved in designing, funding, and implementing. New to this edition: Expanded and updated content in every chapter, with new material on: non-inferiority trials for comparative effectiveness research; incidence-density case-control studies; confounding and effect modification; diagnostic test studies to inform prediction rules; ethical aspects of whole genome sequencing; automated data management approaches; new NIH grant-writing requirements n Color format, and Electronic access, powered by Inkling[trademark] as a free companion to the text; viewable through your browser or as a download to tablet or smartphone; the complete text with optimized navigation; note-sharing, highlighting and bookmarking capability; cross-linking of references and content; and, rapid search options linked to the new glossary.
"About the title" may belong to another edition of this title.