Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

IRB

Showing results (101-110 of 778) with videos related to

Pageof 78
Sort By:
IRB|March 1, 1992
A survey of IRB concerns about social and behavioral researchJoan E Sieber, Reuel M Baluyot
IRB|September 1, 1991
The federal policy for the protection of human subjectsJoan P Porter
IRB|July 1, 1990
Is the practice of offering finder's fees for subject recruitment appropriate? Is the practice widespread or unique to my institution? What is the proper role of the IRB? What is the role of the institution?
IRB|November 1, 1990
A pilot project: bioethics consultants as non-voting members of IRBs at the National Institutes of HealthEvan G DeRenzo, Alison Wichman
IRB|May 1, 1990
Informed consent documents: increasing comprehension by reducing reading levelDaniel R Young, Donald T Hooker, Fred E Freeberg
IRB|July 1, 1992
AIDS and the FDA: an ethical case for limiting patient access to new medical therapiesAndrew F Shorr
IRB|July 1, 1992
Divide and ruleRichard H Nicholson
IRB|July 1, 1992
Demarcating research and treatment interventions: a case illustrationJacquelyn L Goldberg, Jeffrey O Phillips, Benjamin Freedman, et al.
IRB|July 1, 1992
Source data verification in clinical trials involving the temporarily incapacitated subject: is there a missing link in the notion of proxy consent?John R Wilson
IRB|January 1, 1993
Some problems related to risk-benefit assessments in clinical testing of new vaccinesGunnar Bjune, Truls W Gedde-Dahl
Pageof 78

Showing results (101-110 of 778) with videos related to

Sort By:
Pageof 78
IRB|March 1, 1992
A survey of IRB concerns about social and behavioral researchJoan E Sieber, Reuel M Baluyot
IRB|September 1, 1991
The federal policy for the protection of human subjectsJoan P Porter
IRB|July 1, 1990
Is the practice of offering finder's fees for subject recruitment appropriate? Is the practice widespread or unique to my institution? What is the proper role of the IRB? What is the role of the institution?
IRB|November 1, 1990
A pilot project: bioethics consultants as non-voting members of IRBs at the National Institutes of HealthEvan G DeRenzo, Alison Wichman
IRB|May 1, 1990
Informed consent documents: increasing comprehension by reducing reading levelDaniel R Young, Donald T Hooker, Fred E Freeberg
IRB|July 1, 1992
AIDS and the FDA: an ethical case for limiting patient access to new medical therapiesAndrew F Shorr
IRB|July 1, 1992
Divide and ruleRichard H Nicholson
IRB|July 1, 1992
Demarcating research and treatment interventions: a case illustrationJacquelyn L Goldberg, Jeffrey O Phillips, Benjamin Freedman, et al.
IRB|July 1, 1992
Source data verification in clinical trials involving the temporarily incapacitated subject: is there a missing link in the notion of proxy consent?John R Wilson
IRB|January 1, 1993
Some problems related to risk-benefit assessments in clinical testing of new vaccinesGunnar Bjune, Truls W Gedde-Dahl
Pageof 78