Band 1
Management of Data in Clinical Trials
Aus der Reihe
Wiley Series in Probability and Statistics
Fr. 111.00
inkl. gesetzl. MwSt.Beschreibung
Produktdetails
Format
Kopierschutz
Ja
Family Sharing
Nein
Text-to-Speech
Nein
Erscheinungsdatum
30.07.2007
Verlag
Wiley-IEEE PressSeitenzahl
288 (Printausgabe)
Dateigröße
996 KB
Auflage
2. Auflage
Sprache
Englisch
EAN
9780470181270
A valuable new edition of the trusted, practical guide to managing
data in clinical trials
Regardless of size, type, or complexity, accurate results for any
clinical trial are ultimately determined by the quality of the
collected data. Management of Data in Clinical Trials, Second
Edition explores data management and trial organization as the keys
to developing an accurate and reliable clinical trial. With a focus
on the traditional aspects of data collection as well as recent
advances in technology, this new edition provides a complete and
accessible guide to the management structure of a clinical trial,
from planning and development to design and analysis. Practical
approaches that result in the collection of complete and timely
data are also provided.
While maintaining a comprehensive overview of the knowledge and
tools that are essential for the organization of a modern clinical
trial, the author has expanded the topical coverage in the Second
Edition to reflect the possible uses of recent advances in
technology in the data collection process. In addition, the Second
Edition discusses the impact of international regulations governing
the conduct of clinical trials and provides guidelines on ensuring
compliance with national requirements.
Newly featured topics include:
* The growing availability of "off-the-shelf" solutions for
clinical trials
* Potential models for collaboration in the conduct of clinical
trials between academia and the pharmaceutical industry
* The increasing use of the Internet in the collection of data
and management of trials
* Regulatory requirements worldwide and compliance with the ICH
Good Clinical Practice (GCP) Guidelines
* Development of Standard Operating Procedures for the conduct of
clinical trials
Complete with chapter summaries that reinforce key points as
well as over one hundred examples, Management of Data in Clinical
Trials, Second Edition is an ideal resource for practitioners in
the clinical research community who are involved in the development
of clinical trials, including data managers, research associates,
data coordinators, physicians, and statisticians. This book also
serves as an excellent supplemental text for courses in clinical
trials at both the undergraduate and graduate levels.
data in clinical trials
Regardless of size, type, or complexity, accurate results for any
clinical trial are ultimately determined by the quality of the
collected data. Management of Data in Clinical Trials, Second
Edition explores data management and trial organization as the keys
to developing an accurate and reliable clinical trial. With a focus
on the traditional aspects of data collection as well as recent
advances in technology, this new edition provides a complete and
accessible guide to the management structure of a clinical trial,
from planning and development to design and analysis. Practical
approaches that result in the collection of complete and timely
data are also provided.
While maintaining a comprehensive overview of the knowledge and
tools that are essential for the organization of a modern clinical
trial, the author has expanded the topical coverage in the Second
Edition to reflect the possible uses of recent advances in
technology in the data collection process. In addition, the Second
Edition discusses the impact of international regulations governing
the conduct of clinical trials and provides guidelines on ensuring
compliance with national requirements.
Newly featured topics include:
* The growing availability of "off-the-shelf" solutions for
clinical trials
* Potential models for collaboration in the conduct of clinical
trials between academia and the pharmaceutical industry
* The increasing use of the Internet in the collection of data
and management of trials
* Regulatory requirements worldwide and compliance with the ICH
Good Clinical Practice (GCP) Guidelines
* Development of Standard Operating Procedures for the conduct of
clinical trials
Complete with chapter summaries that reinforce key points as
well as over one hundred examples, Management of Data in Clinical
Trials, Second Edition is an ideal resource for practitioners in
the clinical research community who are involved in the development
of clinical trials, including data managers, research associates,
data coordinators, physicians, and statisticians. This book also
serves as an excellent supplemental text for courses in clinical
trials at both the undergraduate and graduate levels.
Noch keine Bewertungen vorhanden
Verfassen Sie die erste Bewertung zu diesem Artikel
Helfen Sie anderen Kundinnen und Kunden durch Ihre Meinung.