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Understanding Clinical Research (Paperback, Ed)
Loot Price: R1,796
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Understanding Clinical Research (Paperback, Ed)
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Publisher's Note: Products purchased from Third Party sellers are
not guaranteed by the publisher for quality, authenticity, or
access to any online entitlements included with the product. A
complete guide to understanding and applying clinical research
resultsIdeal 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 weaknesseswith 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 theimpact
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
General
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