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IRB
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January 1, 1986
A single subject in multiple protocols: is the risk equitable?
Douglas P Lackey
IRB
|
March 1, 1986
The NIH report of its review of the Baby Fae case
F William Dommel,
IRB
|
March 1, 1986
Baby Fae and the media: how the law allows appropriate access
Nicholas Christakis, Morris Panner
IRB
|
September 1, 1996
College on Problems of Drug Dependence policy on administering drugs with abuse potential in human research
IRB
|
November 1, 1996
Psychology faculty satisfaction and compliance with IRB procedures
Becky J Liddle, Elizabeth W Brazelton
IRB
|
October 20, 2001
Reducing postmortem examination refusal by families of research subjects
Jennifer M Phillips
IRB
|
January 1, 1990
Protecting human subjects from harm through improved risk judgments
Eric M Meslin
IRB
|
May 1, 1993
Improving the readability of informed consent documents
Beverly Heinze-Lacey, Carol Saunders, Alan Sugar
IRB
|
May 1, 1993
Ethical, legal, and political problems affecting epidemiology in European countries
Claes-Göran Westrin
IRB
|
January 1, 1994
Multicenter trials and subject eligibility: should local IRBs play a role?
Benjamin Freedman
Page
of 78
Search research articles
Search
Showing results (131-140 of 778) with videos related to
Sort By:
Page
of 78
IRB
|
January 1, 1986
A single subject in multiple protocols: is the risk equitable?
Douglas P Lackey
IRB
|
March 1, 1986
The NIH report of its review of the Baby Fae case
F William Dommel,
IRB
|
March 1, 1986
Baby Fae and the media: how the law allows appropriate access
Nicholas Christakis, Morris Panner
IRB
|
September 1, 1996
College on Problems of Drug Dependence policy on administering drugs with abuse potential in human research
IRB
|
November 1, 1996
Psychology faculty satisfaction and compliance with IRB procedures
Becky J Liddle, Elizabeth W Brazelton
IRB
|
October 20, 2001
Reducing postmortem examination refusal by families of research subjects
Jennifer M Phillips
IRB
|
January 1, 1990
Protecting human subjects from harm through improved risk judgments
Eric M Meslin
IRB
|
May 1, 1993
Improving the readability of informed consent documents
Beverly Heinze-Lacey, Carol Saunders, Alan Sugar
IRB
|
May 1, 1993
Ethical, legal, and political problems affecting epidemiology in European countries
Claes-Göran Westrin
IRB
|
January 1, 1994
Multicenter trials and subject eligibility: should local IRBs play a role?
Benjamin Freedman
Page
of 78