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Clinical research professionals need a direct, practical guide to working together to protect human research subjects. This book is a reference for research sponsors, investigators, and IRB members, with documents created by the Biomedical Research Alliance of New York: - Sample More...pediatric subject assent form - Sample HIPAA authorization form - Sample assent form for genetic testing and/or tissue banking - Sample evaluation/feedback tool for educational programs - Glossary of lay terms for preparing informed-consent documents. - Nuremberg Code, Declaration of Helsinki, Belmont Report, the Common Rule are included.

Institutional review boards (Medicine) --- Medical ethics committees