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IRB

Showing results (551-560 of 778) with videos related to

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IRB|October 14, 2006
General clinical research center staff nurse perceptions and behaviors regarding informed consent: results of a national surveyHarvey J Murff, James W Pichert, Daniel W Byrne, et al.
IRB|October 29, 2008
Nonscientist IRB members at the NIHRobert D Allison, Lura J Abbott, Alison Wichman
IRB|June 26, 2009
An intervention to improve cancer patients' understanding of early-phase clinical trialsNancy E Kass, Jeremy Sugarman, Amy M Medley, et al.
IRB|June 26, 2009
Problems with minimal-risk research oversight: a threat to academic freedom?Lisa M Rasmussen
IRB|June 26, 2009
Data-sharing dilemmas: allowing pharmaceutical company access to research dataJames R Anderson, Toby L Schonfeld
IRB|January 6, 2009
The antidepressant debate and ethically defensible placebo-controlled trialsDuff R Waring
IRB|November 2, 2010
When will we learn?Alan Meisel
IRB|February 22, 2013
Maximizing safety in clinical and translational researchJeremy Sugarman
IRB|December 22, 2011
How should risks and benefits be balanced in research involving pregnant women and fetuses?Carson Strong
IRB|December 22, 2011
Parents' perspectives on the consent approach for minimal-risk research involving childrenMelissa A Cameron, Lauren E Marsillio, Linda F Cushman, et al.
Pageof 78

Showing results (551-560 of 778) with videos related to

Sort By:
Pageof 78
IRB|October 14, 2006
General clinical research center staff nurse perceptions and behaviors regarding informed consent: results of a national surveyHarvey J Murff, James W Pichert, Daniel W Byrne, et al.
IRB|October 29, 2008
Nonscientist IRB members at the NIHRobert D Allison, Lura J Abbott, Alison Wichman
IRB|June 26, 2009
An intervention to improve cancer patients' understanding of early-phase clinical trialsNancy E Kass, Jeremy Sugarman, Amy M Medley, et al.
IRB|June 26, 2009
Problems with minimal-risk research oversight: a threat to academic freedom?Lisa M Rasmussen
IRB|June 26, 2009
Data-sharing dilemmas: allowing pharmaceutical company access to research dataJames R Anderson, Toby L Schonfeld
IRB|January 6, 2009
The antidepressant debate and ethically defensible placebo-controlled trialsDuff R Waring
IRB|November 2, 2010
When will we learn?Alan Meisel
IRB|February 22, 2013
Maximizing safety in clinical and translational researchJeremy Sugarman
IRB|December 22, 2011
How should risks and benefits be balanced in research involving pregnant women and fetuses?Carson Strong
IRB|December 22, 2011
Parents' perspectives on the consent approach for minimal-risk research involving childrenMelissa A Cameron, Lauren E Marsillio, Linda F Cushman, et al.
Pageof 78