An edition of Reviewing clinical trials (2010)

Reviewing clinical trials

a guide for the Ethics Committee

Reviewing clinical trials
Inc Washington (D.C.). Associa ...
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Last edited by MARC Bot
August 22, 2024 | History
An edition of Reviewing clinical trials (2010)

Reviewing clinical trials

a guide for the Ethics Committee

The idea for this manual came from Pfizer in the US, which provided the Clinical Trials Centre at The University of Hong Kong, Hong Kong SAR, PR China with a nonbinding grant for its development. The general project layout protocol was accepted by Pfizer in July 2009. Pfizer has not in any way interfered with the project, except for providing nonbinding comments to the final product. The entire text of this manual was written by Johan PE Karlberg. Marjorie A Speers provided considerable and essential comments on the contents and the first and subsequent drafts. A group of international human research protection experts mostly working in non-profit institutions or organisations - see Contributors for details - reviewed and provided important comments on the contents and final draft. It was solely created with the intention to promote human research protection of participants in clinical trials. This manual will be translated into numerous languages and is provided free of charge as an electronic file over the Internet (http://www.ClinicalTrialMagnifier.com) and offered in print for a fee. The objective beyond this project is to establish educational activities, developed around the manual, and jointly organised with leading academic institutions worldwide.

Publish Date
Publisher
Karlberg
Language
English
Pages
153

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Book Details


Table of Contents

Chapter 1. Introduction. 1.1 Ethics and Bioethics
1.2 Clinical Trials in the Context of Biomedical Research
1.3 Clinical Trial Players and Their Responsibilities
- Chapter 2. Features of Clinical Trials. 2.1 Objectives of Clinical Trials
2.2 Clinical Trial Design
2.3 Controls of Clinical Trials
2.4 Clinical Trial Outcome/Endpoint
2.5 Randomisation
2.6 Blinding
2.7 Sample Size
2.8 Trial Phases
2.9 Multicentre Trials
- Chapter 3. Science, Ethics and Quality Assurance of Clinical Trials. 3.1 Research in Humans
3.2 Science of Clinical Trials
3.3 Issues of Ethics of Clinical Trials
3.4 Issues of EC Procedures
3.5 Quality Assurance of Clinical
3.6 Human Research Protection Programme Accreditation
3.7 The AAHRPP Accreditation Standards
- Chapter 4. Scenarios of Ethics Committee Review
4.1 Introduction to Practical EC Review.

Edition Notes

Also issued online in Pdf via thw World Wide Web.

Published in
Hong Kong, China
Other Titles
Clinical trials

Classifications

Library of Congress
R853.H8 R48 2010

The Physical Object

Pagination
153 p.
Number of pages
153

Edition Identifiers

Open Library
OL53450819M
ISBN 10
9881904110
ISBN 13
9789881904119
OCLC/WorldCat
624759550

Work Identifiers

Work ID
OL39264474W

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August 22, 2024 Created by MARC Bot import new book