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Principles and Practice of Clinical Research

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Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

01.06.2012

Herausgeber

Gallin John I. + weitere

Verlag

Academic Press

Seitenzahl

790

Maße (L/B/H)

28,4/22,2/3,2 cm

Gewicht

1860 g

Auflage

3. Auflage

Sprache

Englisch

ISBN

978-0-12-382167-6

Beschreibung

Rezension

PRAISE FOR THE FIRST EDITION: "...much needed and provides essentially all of the basic information required by investigators involved in clinical research. ...an important resource for institutional libraries..."-THE NEW ENGLAND JOURNAL OF MEDICINE "...it really is a step-by-step DIY book for the uninitiated proposal writer. Full of practical advice, top tips and the ever-useful 'Supplemental reading' section, it even has a sample face sheet and a study design 'tick list'."--IMMUNOLOGY NEWS
"Principles and Practice of Clinical Research, 3 rd Edition is 80% larger than the second edition. Most of the authors are with the National Institutes of Health, but the material is largely applicable to both government- and industry-funded research.This book has been selected for The First Clinical Research Bookshelf, essential reading for clinical research professionals."--Journal of Clinical Research Best Practices, May 2013

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

01.06.2012

Herausgeber

Verlag

Academic Press

Seitenzahl

790

Maße (L/B/H)

28,4/22,2/3,2 cm

Gewicht

1860 g

Auflage

3. Auflage

Sprache

Englisch

ISBN

978-0-12-382167-6

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

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  • Produktbild: Principles and Practice of Clinical Research
  • Produktbild: Principles and Practice of Clinical Research

  • ¿A Historical Perspective on Clinical Research
    ETHICAL, REGULATORY, AND LEGAL ISSUES
    ¿Ethical Principles in Clinical Research
    ¿Researching a Bioethical Question
    ¿Integrity in Research: Individual and Institutional Responsibility
    ¿Institutional Review Boards
    ¿Data and Safety Monitoring Boards
    ¿Data Management in Clinical Trials
    ¿Unanticipated Risks in Clinical Research
    ¿The Regulation of Drugs and Biological Products by the Food and Drug Administration
    ¿Legal Issues
    ¿Rules to Prevent Conflict of Interest for Clinical Investigators Conducting Human Subjects Research
    ¿National Institutes of Health Policy on the Inclusion of Women and Minorities as Subjects in Clinical Research
    ¿Clinical Research: A Patient Perspective
    ¿The Clinical Researcher and the Media
    BIOSTATISTICS AND EPIDEMIOLOGY
    ¿An Introduction to Biostatistics: Randomization, Hypothesis Testing, and Sample Size Estimation
    ¿Design and Conduct of Observational Studies and Clinical Trials
    ¿Small Clinical Trials
    ¿Large Clinical Trials and Registries - Clinical Research Institutes
    ¿Using Secondary Data in Statistical Analysis
    ¿An Introduction to Survival Analysis
    ¿Measures of Function and Health-Related Quality of Life
    TECHNOLOGY TRANSFER, PROTOCOL DEVELOPMENT, FUNDING AND OTHER ISSUES
    ¿Overview of Technology Development
    ¿Technology Transfer
    ¿Writing a Protocol
    ¿Evaluating a Protocol Budget
    ¿Data Management in Clinical Research: General Principles and a Guide to Sources
    ¿Getting the Funding You Need to Support Your Research: Navigating the National Institutes of Health Peer Review Process
    ¿Clinical Research from the Industry Perspective
    ¿Human Genome Project, Genomics, and Clinical Research