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Understanding Clinical Research

Understanding Clinical Research

9780071746786
294,78 zł
280,04 zł Zniżka 14,74 zł Brutto
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Opis

Publishers 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 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 studys 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

Szczegóły produktu
53697
9780071746786
9780071746786

Opis

Rok wydania
2013
Numer wydania
1
Oprawa
miękka foliowana
Liczba stron
272
Wymiary (mm)
163 x 226
Waga (g)
365
  • INTRODUCTION

    ETHICS IN CLINICAL RESEARCH

    THE RESEARCH QUESTION

    DESIGNS and TYPES OF STUDIES

    STARTING THE STUDY

    RECRUITMENT OF SUBJECTS

    DATA MANAGEMENT

    DATA ANALYSIS

    CLOSE OUT

    REPORTING AND INTERPRETING FINDINGS

    APPENDICES

    Statistics Tables

    Summary of Statistical Procedures

    Power and Sample size

    Effect size index

    Power for ANOVA

    Power for Correlations

    Power for Regressions

    Power for chi-square

    Transformation of Data

    Sample Informed consent form

    Glossary of terms

    Glossary of statistical symbols and abbreviations

    Industry Resources

    Associations

    Conference Organizers

    Publishers

    Top Sponsors

    Top CROs

    Performance measures

    Speed

    Quality

    Cost

    Declaration of Helsinki

    FDA form 1572

    Financial Disclosure form

    Code of Federal Regulations

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