Designing Clinical Research,New

Designing Clinical Research,New

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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 readerfriendly 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: noninferiority trials for comparative effectiveness research incidencedensity casecontrol studies confounding and effect modification diagnostic test studies to inform prediction rules ethical aspects of whole genome sequencing automated data management approaches new NIH grantwriting requirements Color format, and Electronic access, powered by Inkling 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 notesharing, highlighting and bookmarking capability crosslinking of references and content rapid search options linked to the new glossary

⚠️ WARNING (California Proposition 65):

This product may contain chemicals known to the State of California to cause cancer, birth defects, or other reproductive harm.

For more information, please visit www.P65Warnings.ca.gov.

  • Q: What is the primary focus of 'Designing Clinical Research'? A: The primary focus of 'Designing Clinical Research' is to provide a practical guide for health professionals involved in clinical, translational, and public health research, presenting advanced epidemiologic concepts in an accessible manner.
  • Q: What are some key updates in the fourth edition of this book? A: The fourth edition includes expanded and updated content in every chapter, highlighting topics such as non-inferiority trials, incidence-density case-control studies, confounding effects, ethical aspects of genome sequencing, and new NIH grant-writing requirements.
  • Q: Who is the author of 'Designing Clinical Research'? A: The author of the book is Dr. Stephen B. Hulley, MD, MPH, who is renowned for his contributions to clinical research methodology.
  • Q: Is there an electronic version available for this book? A: Yes, the book is available in an electronic format powered by Inkling™, which offers a complete text viewable through browsers or downloadable to tablets and smartphones.
  • Q: How many pages does 'Designing Clinical Research' have? A: The book contains a total of 378 pages.
  • Q: What type of binding does this book have? A: The book is available in a paperback binding.
  • Q: What condition is the book in? A: The book is listed as being in 'Good' condition.
  • Q: What category does this book fall under? A: The book falls under the 'Public Health' category.
  • Q: When was 'Designing Clinical Research' published? A: The book was published on July 10, 2013.
  • Q: What features are included in the electronic access of the book? A: The electronic access includes optimized navigation, note-sharing, highlighting, bookmarking capability, cross-linking of references, and rapid search options connected to a new glossary.

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