Beneficence - Protecting Human Subject Research Participants
Beneficence - Protecting Human Subject Research Participants
Beneficence - Protecting Human Subject Research Participants
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<strong>Protecting</strong> <strong>Human</strong> <strong>Research</strong> <strong>Participants</strong>Respect for PersonsMain Menu | Glossary | HelpInformed ConsentPrevious Page 4 of 25NextThe HHS regulations (45 CFR 46.116) require that investigators obtain legally effective informedconsent from prospective participants in a way that allows them to consider whether or not to participateand that minimizes the possibility for coercion or undue influence .Potential participants must understand that enrolling in the research is voluntary and that they maywithdraw from the study at any time without penalty or loss of benefits (45 CFR 46.116(a)).In order for participation in research to be voluntary, the potential for coercion and undue influence mustbe minimized.Previous Page 4 of 25Nexthttp://phrp.nihtraining.com/respect/04_respect.php6/20/2008 2:09:23 PM
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