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Evaluating the science and ethics of research on humans : a guide for IRB members / Dennis J. Mazur.

By: Publication details: Baltimore : Johns Hopkins University Press, 2007.Description: xi, 252 p. ; 23 cmISBN:
  • 0801885019 (hardcover : alk. paper)
  • 9780801885013 (hardcover : alk. paper)
  • 0801885027 (pbk. : alk. paper)
  • 9780801885020 (pbk. : alk. paper)
Subject(s): DDC classification:
  • WB 60 M476e 2007
Online resources:
Contents:
Contents Introduction. What Can the New IRB Member Expect? Part I. The IRB: Its Work and Its Challenges 1. What Is an IRB, and What Does It Do? 2. Basic Terms and Concepts Used in IRB Work 3. What Is Risk? Part II. The Scientific Protocol and the Informed Consent Form 4. Prescreening: The Quality of the Submitted Materials and the Qualifications of the Research Team 5. The Scientific Protocol 6. The Informed Consent Form 7. Recruitment, Selection, and Compensation of Study Participants 8. Research involving Questionnaires and Surveys 9. Protection of Research Data, Specimens, and Privacy Part III. The Continuing Work of the IRB 10. The Ethics of Scientific Research on Humans 11. Continuing Review, Communication, and Feedback 12. Where Are IRBs Making Mistakes, and How Can We Minimize the Occurrence of Mistakes? 13. Strategies for Managing the IRB Workload and for Protecting IRB Decision Making 14. Decision-Making Capacity and accountability in Research
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Holdings
Item type Current library Call number Copy number Status Date due Barcode
Book Open Access Book Open Access Health Sciences Library WB 60 M476e 2007 (Browse shelf(Opens below)) 1 Available MBAL22040087

Includes bibliographical references (p. 239-245) and index.

Contents

Introduction. What Can the New IRB Member Expect?

Part I. The IRB: Its Work and Its Challenges
1. What Is an IRB, and What Does It Do?
2. Basic Terms and Concepts Used in IRB Work
3. What Is Risk?

Part II. The Scientific Protocol and the Informed Consent Form
4. Prescreening: The Quality of the Submitted Materials and the Qualifications of the Research
Team
5. The Scientific Protocol
6. The Informed Consent Form
7. Recruitment, Selection, and Compensation of Study Participants
8. Research involving Questionnaires and Surveys
9. Protection of Research Data, Specimens, and Privacy

Part III. The Continuing Work of the IRB
10. The Ethics of Scientific Research on Humans
11. Continuing Review, Communication, and Feedback
12. Where Are IRBs Making Mistakes, and How Can We Minimize the Occurrence of Mistakes?
13. Strategies for Managing the IRB Workload and for Protecting IRB Decision Making
14. Decision-Making Capacity and accountability in Research

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