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Preface ix
Introduction / What Can the New IRB Member Expect? 1
The IRB, Its Work, and Its Challenges
What Is an IRB, and What Does It Do? 13
Basic Terms and Concepts Used in IRB Work 33
What Is Risk? 58
The Scientific Protocol and the Informed Consent Form
Prescreening of Proposals 87
The Scientific Protocol 94
The Informed Consent Form 123
Recruitment, Selection, and Compensation of Study Participants 142
Research involving Questionnaires and Surveys 147
Protection of Participants' Privacy in Research Data and Specimens 152
The Continuing Work of the IRB
The Ethical Issues of Informed Consent 167
Continuing Review, Communication, and Feedback 174
Where Are IRBs Making Mistakes, and How Can We Minimize Mistakes? 188
Strategies for Managing the IRB Workload and Supporting IRB Decision Making 196
Decision-Making Capacity and Accountability in Research 205
Summary / The IRB's Key Role 223
A Check List for Reviewing a Scientific Protocol 231
A Check List for Reviewing an Informed Consent Form 237
Notes 239
Website References for Cited Documents 245
Index 247
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Add Evaluating the Science and Ethics of Research on Humans: A Guide for IRB Members, Biomedical research on humans is an important part of medical progress. But, when health and lives are at risk, safety and ethical practices need to be the top priority. The need for the committees that regulate and oversee such research—institutional rev, Evaluating the Science and Ethics of Research on Humans: A Guide for IRB Members to your collection on WonderClub |