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Showing results (401-410 of 778) with videos related to

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IRB|February 12, 2004
Children in research: new perspectives and practices for informed consentMarion E Broome, Eric Kodish, Gail Geller, et al.
IRB|February 12, 2004
Good study design and analysis plans as features of ethical research with humansJanice M Weinberg, Ken P Kleinman
IRB|September 26, 2003
When is informed consent appropriate in educational research?: regulatory and ethical issuesJames M DuBois
IRB|September 26, 2003
"Doing it right--together": study groups & research agendas
IRB|September 26, 2003
"Therapeutic misconception" and "recruiting doublespeak" in the informed consent processMark Hochhauser
IRB|June 19, 2018
The Food and Drug Administration's Federal Review of a Pediatric Muscular Dystrophy ProtocolDonna L Snyder, Robert M Nelson
IRB|October 20, 2001
Attention to difference and women's consent to researchLisa A Eckenwiler
IRB|October 20, 2001
Structuring the review of human genetics protocols, part III: gene therapy studiesKathleen C Glass, Charles Weijer, Denis Cournoyer, et al.
IRB|October 20, 2001
Regulatory orphans: juvenile prisoners as transvulnerable research subjectsJoyce G Reed
IRB|October 20, 2001
A reappraisal of female adolescent participation in drug clinical trialsTerry M VandenBosch, Becky G Ward, Debra Mattison
Pageof 78

Showing results (401-410 of 778) with videos related to

Sort By:
Pageof 78
IRB|February 12, 2004
Children in research: new perspectives and practices for informed consentMarion E Broome, Eric Kodish, Gail Geller, et al.
IRB|February 12, 2004
Good study design and analysis plans as features of ethical research with humansJanice M Weinberg, Ken P Kleinman
IRB|September 26, 2003
When is informed consent appropriate in educational research?: regulatory and ethical issuesJames M DuBois
IRB|September 26, 2003
"Doing it right--together": study groups & research agendas
IRB|September 26, 2003
"Therapeutic misconception" and "recruiting doublespeak" in the informed consent processMark Hochhauser
IRB|June 19, 2018
The Food and Drug Administration's Federal Review of a Pediatric Muscular Dystrophy ProtocolDonna L Snyder, Robert M Nelson
IRB|October 20, 2001
Attention to difference and women's consent to researchLisa A Eckenwiler
IRB|October 20, 2001
Structuring the review of human genetics protocols, part III: gene therapy studiesKathleen C Glass, Charles Weijer, Denis Cournoyer, et al.
IRB|October 20, 2001
Regulatory orphans: juvenile prisoners as transvulnerable research subjectsJoyce G Reed
IRB|October 20, 2001
A reappraisal of female adolescent participation in drug clinical trialsTerry M VandenBosch, Becky G Ward, Debra Mattison
Pageof 78