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IRB

Showing results (51-60 of 778) with videos related to

Pageof 78
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IRB|May 1, 1986
What are the ideal characteristics of unaffiliated/nonscientist IRB members?Joan P Porter
IRB|September 1, 1990
Ensuring that nonscientists and subjects understand research protocolsMuriel Goldhammer, Jacki Altman
IRB|May 1, 1996
The use of normal children as participants in research on therapyBruce Gordon, Ernest Prentice, Paul Reitemeier
IRB|October 20, 2001
Exception from informed consent for emergency research: drawing on existing skills and experienceArlene M Davis
IRB|October 20, 2001
A case study in adolescent participation in clinical research: eleven clinical sites, one common protocol, and eleven IRBsAudrey Smith Rogers, Donald F Schwartz, Gloria Weissman, et al.
IRB|September 1, 1996
Placebo controls are not good scienceCharles Weijer, Paul Appelbaum
IRB|February 1, 1982
The validity of ignorant consent to medical researchBenjamin Freedman
IRB|November 1, 1986
Recontacting subjects in mutagen exposure monitoring studiesDavid B Busch, George T Bryan, Edward M Messing, et al.
IRB|November 1, 1986
Does the moral philosophy of the Belmont Report rest on a mistake?Ernest Marshall
IRB|March 1, 1997
Continuing review of research involving human subjects: approach to the problem and remaining areas of concernBruce Gordon, Ernest Prentice
Pageof 78

Showing results (51-60 of 778) with videos related to

Sort By:
Pageof 78
IRB|May 1, 1986
What are the ideal characteristics of unaffiliated/nonscientist IRB members?Joan P Porter
IRB|September 1, 1990
Ensuring that nonscientists and subjects understand research protocolsMuriel Goldhammer, Jacki Altman
IRB|May 1, 1996
The use of normal children as participants in research on therapyBruce Gordon, Ernest Prentice, Paul Reitemeier
IRB|October 20, 2001
Exception from informed consent for emergency research: drawing on existing skills and experienceArlene M Davis
IRB|October 20, 2001
A case study in adolescent participation in clinical research: eleven clinical sites, one common protocol, and eleven IRBsAudrey Smith Rogers, Donald F Schwartz, Gloria Weissman, et al.
IRB|September 1, 1996
Placebo controls are not good scienceCharles Weijer, Paul Appelbaum
IRB|February 1, 1982
The validity of ignorant consent to medical researchBenjamin Freedman
IRB|November 1, 1986
Recontacting subjects in mutagen exposure monitoring studiesDavid B Busch, George T Bryan, Edward M Messing, et al.
IRB|November 1, 1986
Does the moral philosophy of the Belmont Report rest on a mistake?Ernest Marshall
IRB|March 1, 1997
Continuing review of research involving human subjects: approach to the problem and remaining areas of concernBruce Gordon, Ernest Prentice
Pageof 78