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Understanding Clinical Research, by Renato D. Lopes, Robert A. Harrington
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A complete guide to understanding and applying clinical research results
Ideal for both researchers and healthcare providers
Understanding Clinical Research addresses both the operational challenges of clinical trials and the needs of clinicians to comprehend the nuances of research methods to accurately analyze study results. This timely resource covers all aspects of clinical trials--from study design and statistics to regulatory oversight--and it delivers a detailed yet streamlined overview of must-know research topics.
The text features an accessible three-part organization that traces the evolution of clinical research and explains the bedrock principles and unique challenges of clinical experimentation and observational research. Reinforcing this content are real-life case examples--drawn from the authors' broad experience--that put chapter concepts into action and contribute to a working knowledge of integral research techniques.
FEATURES:
- The most definitive guide to promoting excellence in clinical research, designed to empower healthcare providers to assess a study's strengths and weaknesses with confidence and apply this knowledge to optimize patient outcomes
- In-depth coverage of fundamental research methods and protocols from preeminent authorities provides readers with an instructive primer and a springboard for ongoing clinical research education
- Clear, comprehensive three-part organization:
- Section One: Evolution of Clinical Research offers a succinct history of clinical trials, drug regulations, and the role of the FDA while covering the impact of information technology and academic research organizations
- Section Two: Principles of Clinical Experimentation takes you through the typical phases of clinical trials in the development of medical products, from initial human subject research to postapproval surveillance studies
- Section Three: Observational Research highlights the underlying principles, pitfalls, and methods for case-control studies, cohort studies, registries, and subgroup analyses within randomized trials
- Sales Rank: #1800055 in eBooks
- Published on: 2013-05-22
- Released on: 2013-05-22
- Format: Kindle eBook
Most helpful customer reviews
1 of 1 people found the following review helpful.
A great book, by the masters in clinical research
By Accidental Tourist
Indeed a fantastic book, to everyone interested in the field of clinical research. Also, if you are a physician, a scientist, or a student, it is nice to understand how a new drug gets to be scrutinized before public availability. The text is easy to read, despite being about a very specific field of medicine. The authors have done a great job putting together so many experts in the field of clinical research, and essentially turning this into a immediate classic, a reference book. I can foresee this book as standard reading material to every Masters or PhD student.
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